# GABAPENTIN

NDC: 49483-607
Generic name: GABAPENTIN
Labeler / Manufacturer: TIME CAP LABORATORIES, INC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20151230

FDA application: ANDA090007

## Active ingredients

- GABAPENTIN: 400 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"49483-607"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=49483-607
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=08880902-bd44-41b6-866b-2cbad4c3f2b1