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Atropine Sulfate

NDC 0641-6251 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA213561
Dosage form / routeINJECTION · ENDOTRACHEAL INTRAMEDULLARY INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
Active ingredientsATROPINE SULFATE (.4 mg/mL)
Marketing started20211201
Package count1

External sources

Source: openFDA. Public-domain (CC0).