# GABAPENTIN

NDC: 72737-005
Generic name: GABAPENTIN
Labeler / Manufacturer: STALLION LABORATORIES PRIVATE LIMITED
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20250807

FDA application: ANDA219319

## Active ingredients

- GABAPENTIN: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72737-005"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72737-005
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b26fd0c6-6aab-4957-8a32-cc7adb9b5fc9