FDA NDC Directory · JSON-LD · Markdown

GABAPENTIN

NDC 72737-005 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerSTALLION LABORATORIES PRIVATE LIMITED
Marketing categoryAbbreviated NDA (generic) · App ANDA219319
Dosage form / routeCAPSULE · ORAL
Active ingredientsGABAPENTIN (100 mg/1)
Marketing started20250807
Package count4

External sources

Source: openFDA. Public-domain (CC0).