Regulatory PathRegulatory requirements compared

Active substance

Ampicillin

Open in the medicines table

SFDA Saudi Arabia — SFDA human drug list

Trade nameStrengthForm · routePackPublic priceTypeCompanyStatus
EPICOCILLIN VIAL 1G1 gpowder for solution for injection · Intravenous use1 VialSAR 9.05Generic · PrescriptionEIPICOValid
EPICOCILLIN VIAL 500MG500 mgpowder for solution for injection · Intravenous use1 VialSAR 6.45Generic · PrescriptionEIPICOValid
STANDACILLIN 1G VIAL WITH SOLVENT1 gPowder and solvent for solution for injection/infusion · Intravenous use1 VialSAR 14.65Generic · PrescriptionSANDOZValid
STANDACILLIN 500MG INJ WITH SOLVENT500 mgPowder and solvent for solution for injection/infusion · Intravenous use1 VialSAR 7.75Generic · PrescriptionSANDOZValid
AMPICILLIN 1GM POWDER FOR IV AND IM INJECTION1 gpowder for solution for injection · Intramuscular and intravenous use50 VialSAR 198.85Generic · PrescriptionANTIBIOTIC S.EWithdrawn by MAH · Not Marketed
AMPICILLIN 500MG POWDER FOR IV AND IM INJECTION500 mgpowder for solution for injection · Intramuscular and intravenous use50 VialSAR 147.40Generic · PrescriptionANTIBIOTIC S.EWithdrawn by MAH · Not Marketed
PENBRITIN VIAL 250 MG250 mgSolution · Intravenous use10 VialSAR 35.65NCE · PrescriptionSMIITHKLINE BEECHAMWithdrawn by MAH · Not Marketed
Indications — CHI Daman Drug Formulary

ACUTE PANCREATITIS; ACUTE PYELONEPHRITIS; BACTERIAL MENINGITIS; BACTRIAL INFECTIONS OF THE GASTROINTESTINAL TRACT - SHIGELLA INFECTIONS; BACTRIAL INFECTIONS OF THE GASTROINTESTINAL TRACT - TYPHOID AND PARATYPHOID FEVERS; COMMUNITY ACQUIRED PNEUMONEA; ENDOCARDITIS; INTRA-ABDOMINAL INFECTIONS; MATERNAL AND CHILD HEALTHCARE- PROPHYLAXIS FOR P-PROM, DELIVERY BY C-SECTION, GROUP B STREPTOCOCCUS; OSTEOMYELITIS; PERITONITIS; PREVENTION AND CHEMOPROPHYLAXIS OF BACTERIAL MENINGITIS- STREPTOCOCCUS B CARRIER STATE COMPLICATING PREGNANCY, CHILDBIRTH AND THE PUERPERIUM; Pyogenic Arthritis; RECURRENT URINARY TRACT INFECTIONS (UTI); TRAVEL RELATED INFECTIONS-TREATMENT

US FDA United States — FDA approvals (Drugs@FDA)

ProductStrengthForm · routeApplicantStatusFirst approved
AMPICILLIN SODIUMEQ 125MG BASE/VIAL; EQ 250MG BASE/VIAL; EQ 500MG BASE/VIAL; EQ 1GM BASE/VIAL; EQ 2GM BASE/VIAL; EQ 10GM BASE/VIALinjectable · injectionSANDOZPrescription3 Mar 1971
AMPICILLIN SODIUMEQ 250MG BASE/VIAL; EQ 1GM BASE/VIAL; EQ 500MG BASE/VIALinjectable · injectionACS DOBFAR SPAPrescription12 May 1987
AMPICILLIN SODIUMEQ 1GM BASE/VIAL; EQ 2GM BASE/VIAL; EQ 250MG BASE/VIAL; EQ 500MG BASE/VIALinjectable · injectionHQ SPECLT PHARMAPrescription15 Apr 1993
AMPICILLIN SODIUMEQ 10GM BASE/VIALinjectable · injectionHQ SPECLT PHARMAPrescription15 Apr 1993
AMPICILLIN SODIUMEQ 2GM BASE/VIALinjectable · injectionACS DOBFAR SPAPrescription12 Jul 1993
AMPICILLIN SODIUMEQ 250MG BASE/VIAL; EQ 500MG BASE/VIAL; EQ 1GM BASE/VIAL; EQ 2GM BASE/VIALinjectable · injectionANTIBIOTICEPrescription28 Dec 2009
AMPICILLIN SODIUMEQ 10GM BASE/VIALinjectable · injectionEUGIA PHARMA SPECLTSPrescription17 Aug 2010
AMPICILLIN SODIUMEQ 250MG BASE/VIAL; EQ 500MG BASE/VIAL; EQ 1GM BASE/VIAL; EQ 2GM BASE/VIALinjectable · injectionEUGIA PHARMA SPECLTSPrescription17 Aug 2010
AMPICILLIN SODIUMEQ 10GM BASE/VIALinjectable · injectionACS DOBFAR SPAPrescription3 Apr 2013
AMPICILLIN SODIUMEQ 10GM BASE/VIALinjectable · injectionACS DOBFAR SPAPrescription20 Dec 2013
AMPICILLIN SODIUMEQ 10GM BASE/VIALinjectable · injectionONESOURCE SPECIALTYPrescription7 Apr 2014
AMPICILLIN SODIUMEQ 1GM BASE/VIAL; EQ 2GM BASE/VIALinjectable · injectionONESOURCE SPECIALTYPrescription9 Apr 2014
AMPICILLIN SODIUMEQ 10GM BASE/VIALinjectable · injectionSAGENT PHARMS INCPrescription20 Oct 2015
AMPICILLIN SODIUMEQ 125MG BASE/VIAL; EQ 250MG BASE/VIAL; EQ 500MG BASE/VIAL; EQ 1GM BASE/VIAL; EQ 2GM BASE/VIALinjectable · injectionSAGENT PHARMS INCPrescription27 Nov 2015
PENBRITIN-SEQ 125MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**; EQ 250MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**; EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**; EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**; EQ 2GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**; EQ 4GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**injectable · injectionWYETH AYERSTDiscontinued29 Dec 1966
AMPICILLIN SODIUMEQ 125MG BASE/VIAL; EQ 250MG BASE/VIAL; EQ 500MG BASE/VIAL; EQ 1GM BASE/VIAL; EQ 2GM BASE/VIAL; EQ 10GM BASE/VIALinjectable · injectionHIKMADiscontinued24 Jun 1986
TOTACILLIN-NEQ 1GM BASE/VIAL; EQ 2GM BASE/VIALinjectable · injectionGLAXOSMITHKLINEDiscontinued19 Dec 1986
AMPICILLIN SODIUMEQ 1GM BASE/VIAL; EQ 2GM BASE/VIALpowder · intravenousSANDOZDiscontinued19 Feb 1987
AMPICILLIN SODIUMEQ 10GM BASE/VIALinjectable · injectionWATSON LABS INCDiscontinued15 Sep 1988
AMPICILLIN SODIUMEQ 125MG BASE/VIAL; EQ 250MG BASE/VIAL; EQ 500MG BASE/VIAL; EQ 1GM BASE/VIAL; EQ 2GM BASE/VIALinjectable · injectionWATSON LABS INCDiscontinued28 Oct 1988
AMPICILLIN SODIUMEQ 1GM BASE/VIAL; EQ 2GM BASE/VIAL; EQ 125MG BASE/VIAL; EQ 500MG BASE/VIALinjectable · injectionHQ SPECLT PHARMADiscontinued15 Apr 1993
AMPICILLIN SODIUMEQ 500MG BASE/VIALinjectable · injectionHANFORD GCDiscontinued15 Apr 1993
AMPICILLIN SODIUMEQ 125MG BASE/VIALinjectable · injectionACS DOBFAR SPADiscontinued12 Jul 1993
AMPICILLIN SODIUMEQ 125MG BASE/VIALinjectable · injectionEUGIA PHARMA SPECLTSDiscontinued17 Aug 2010
AMPICILLIN SODIUMEQ 500MG BASE/VIAL; EQ 1GM BASE/VIAL; EQ 2GM BASE/VIALinjectable · injectionACS DOBFAR SPADiscontinued3 Apr 2013

11 more — full table

Canada Canada — marketed products (Health Canada)

BrandDINStrengthForm · routeCompany
AMPICILLIN FOR INJECTION, USP022269952 G / VIALPOWDER FOR SOLUTION · INTRAVENOUSFRESENIUS KABI CANADA LTD
AMPICILLIN FOR INJECTION, USP022270021 G / VIALPOWDER FOR SOLUTION · INTRAMUSCULAR; INTRAVENOUSFRESENIUS KABI CANADA LTD
AMPICILLIN FOR INJECTION, USP02227010500 MG / VIALPOWDER FOR SOLUTION · INTRAMUSCULAR; INTRAVENOUSFRESENIUS KABI CANADA LTD
AMPICILLIN FOR INJECTION, USP02227029250 MG / VIALPOWDER FOR SOLUTION · INTRAVENOUS; INTRAMUSCULARFRESENIUS KABI CANADA LTD
AMPICILLIN SODIUM FOR INJECTION BP02462303250 MG / VIALPOWDER FOR SOLUTION · INTRAMUSCULAR; INTRAVENOUSAURO PHARMA INC
AMPICILLIN SODIUM FOR INJECTION BP02462311500 MG / VIALPOWDER FOR SOLUTION · INTRAMUSCULAR; INTRAVENOUSAURO PHARMA INC
AMPICILLIN SODIUM FOR INJECTION BP024623381 G / VIALPOWDER FOR SOLUTION · INTRAMUSCULAR; INTRAVENOUSAURO PHARMA INC
AMPICILLIN SODIUM FOR INJECTION BP024623462 G / VIALPOWDER FOR SOLUTION · INTRAVENOUSAURO PHARMA INC
AMPICILLIN SODIUM FOR INJECTION BP02530481500 MG / VIALPOWDER FOR SOLUTION · INTRAVENOUS; INTRAMUSCULAREUGIA PHARMA INC.
AMPICILLIN SODIUM FOR INJECTION BP025305031 G / VIALPOWDER FOR SOLUTION · INTRAVENOUS; INTRAMUSCULAREUGIA PHARMA INC.
AMPICILLIN SODIUM FOR INJECTION BP025305112 G / VIALPOWDER FOR SOLUTION · INTRAVENOUSEUGIA PHARMA INC.
AMPICILLIN SODIUM FOR INJECTION, USP00872644250 MG / VIALPOWDER FOR SOLUTION · INTRAMUSCULAR; INTRAVENOUSTEVA CANADA LIMITED
AMPICILLIN SODIUM FOR INJECTION, USP00872652500 MG / VIALPOWDER FOR SOLUTION · INTRAVENOUS; INTRAMUSCULARTEVA CANADA LIMITED
AMPICILLIN SODIUM FOR INJECTION, USP019333451 G / VIALPOWDER FOR SOLUTION · INTRAVENOUS; INTRAMUSCULARTEVA CANADA LIMITED
AMPICILLIN SODIUM FOR INJECTION, USP019333532 G / VIALPOWDER FOR SOLUTION · INTRAMUSCULAR; INTRAVENOUSTEVA CANADA LIMITED
TEVA-AMPICILLIN00020877250 MGCAPSULE · ORALTEVA CANADA LIMITED
TEVA-AMPICILLIN00020885500 MGCAPSULE · ORALTEVA CANADA LIMITED

Prices — United States and England

SourceProduct as listedPriceUnit / packDate
US NADACAMPICILLIN 500 MG CAPSULE$0.44112per EA23 Sep 2026
NHS Drug TariffAmpicillin 500mg capsules£47.9628 capsule1 Oct 2026

NADAC: average price US retail pharmacies pay to buy the medicine. NHS Drug Tariff Part VIIIA: basic price reimbursed to pharmacies in England and Wales.

WHO WHO Model List of Essential Medicines (2025)

  • 6.2.1. Access group antibiotics · core
    First choice: Bacterial pneumonia (Community-acquired pneumonia - severe) [children]; First choice: Acute malnutrition in infants, children or adolescents (complicated) [children]; First choice: Sepsis without septic shock (co-prescribed with gentamicin); First choice: Peritoneal abscess (mild-moderate) (co-prescribed with gentamicin); First choice: Peritoneal abscess (severe) (co-prescribed with gentamicin); First choice: Peritonitis (mild-moderate) (co-prescribed with gentamicin); First choice: Peritonitis (severe) (co-prescribed with gentamicin); Second choice: Bacterial meningitis
    Parenteral > General injections > unspecified: 500 mg in vial (as sodium salt) powder for injection (EMLc); 1 g in vial (as sodium salt) powder for injection (EMLc) | Parenteral > General injections > unspecified: 500 mg in vial (as sodium salt) powder for injection; 1 g in vial (as sodium salt) powder for injection
  • 5.1.6.1. Medicines for bacterial central nervous system infections · core
    Second choice: Bacterial meningitis
    Parenteral > General injections > unspecified: 500 mg in vial (as sodium salt) powder for injection; 1 g in vial (as sodium salt) powder for injection

Safety signals and safety-related labeling changes

All safety entries for ampicillin →

Combinations containing Ampicillin

Values as published by each source: SFDA human drug list (4-2026, as published by the Council of Health Insurance; indications from the CHI Daman Drug Formulary), Drugs@FDA, EMA medicines data, Health Canada Drug Product Database (Open Government Licence – Canada), CMS NADAC, NHS Drug Tariff Part VIIIA (NHSBSA Copyright, Open Government Licence v3.0), WHO Model List of Essential Medicines (CC BY 3.0 IGO; regrouped by active substance, not created by WHO), EMA PRAC, US FDA safety-related labeling changes and MHRA Drug Safety Update (Open Government Licence v3.0). Sources and reuse. Not a substitute for the official registers or the product information.