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Octreotide Acetate

NDC 71288-566 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerMeitheal Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA075957
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS SUBCUTANEOUS
Active ingredientsOCTREOTIDE ACETATE (50 ug/mL)
Marketing started20250228
Package count1

External sources

Source: openFDA. Public-domain (CC0).