FDA NDC Directory · JSON-LD · Markdown

ATROPINE SULFATE

NDC 51662-1619 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerHF Acquisition Co LLC, DBA HealthFirst
Marketing categoryAbbreviated NDA (generic) · App ANDA213561
Dosage form / routeINJECTION · ENDOTRACHEAL INTRAMEDULLARY INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
Active ingredientsATROPINE SULFATE (.4 mg/mL)
Marketing started20221001
Package count2

External sources

Source: openFDA. Public-domain (CC0).