FDA NDC Directory · JSON-LD · Markdown

ATROPINE SULFATE

NDC 51662-1289 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerHF Acquisition Co LLC, DBA HealthFirst
Marketing categoryNew Drug Application (innovator) · App NDA021146
Dosage form / routeINJECTION, SOLUTION · ENDOTRACHEAL INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
Active ingredientsATROPINE SULFATE (.1 mg/mL)
Marketing started20180923
Package count2

External sources

Source: openFDA. Public-domain (CC0).