Active substance
Gonadotropin chorionic
- US FDA 12
- Safety 1
US FDA United States — FDA approvals (Drugs@FDA)
| Product | Strength | Form · route | Applicant | Status | First approved |
|---|---|---|---|---|---|
| CHORIONIC GONADOTROPIN | 10,000 UNITS/VIAL | injectable · injection | FRESENIUS KABI USA | Prescription | 5 Mar 1973 |
| CHORIONIC GONADOTROPIN | 5,000 UNITS/VIAL; 10,000 UNITS/VIAL | injectable · injection | FERRING | Prescription | 15 Jan 1974 |
| PREGNYL | 10,000 UNITS/VIAL | injectable · injection | ORGANON USA LLC | Prescription | 20 Oct 1976 |
| CHORIONIC GONADOTROPIN | 5,000 UNITS/VIAL; 20,000 UNITS/VIAL; 15,000 UNITS/VIAL | injectable · injection | FRESENIUS KABI USA | Discontinued | 5 Mar 1973 |
| CHORIONIC GONADOTROPIN | 20,000 UNITS/VIAL; 2,000 UNITS/VIAL; 15,000 UNITS/VIAL | injectable · injection | FERRING | Discontinued | 15 Jan 1974 |
| CHORIONIC GONADOTROPIN | 5,000 UNITS/VIAL; 10,000 UNITS/VIAL | injectable · injection | BEL MAR | Discontinued | 26 Mar 1974 |
| A.P.L. | 5,000 UNITS/VIAL; 10,000 UNITS/VIAL; 20,000 UNITS/VIAL | injectable · injection | FERRING | Discontinued | 13 Dec 1974 |
| CHORIONIC GONADOTROPIN | 5,000 UNITS/VIAL | injectable · injection | QUAD PHARMS | Discontinued | |
| CHORIONIC GONADOTROPIN | 5,000 UNITS/VIAL | injectable · injection | QUAD PHARMS | Discontinued | |
| CHORIONIC GONADOTROPIN | 10,000 UNITS/VIAL | injectable · injection | QUAD PHARMS | Discontinued | |
| CHORIONIC GONADOTROPIN | 10,000 UNITS/VIAL | injectable · injection | QUAD PHARMS | Discontinued | |
| CHORIONIC GONADOTROPIN | 20,000 UNITS/VIAL | injectable · injection | QUAD PHARMS | Discontinued |
Safety signals and safety-related labeling changes
- US FDA 2 Mar 2023 PREGNYL — safety-related labeling change
Labeling sections changed: Contraindications; Warnings and Precautions; Adverse Reactions; Use in Specific Populations
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.