# Gabapentin

NDC: 17856-0600
Generic name: gabapentin
Labeler / Manufacturer: ATLANTIC BIOLOGICALS CORP.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20180629

FDA application: ANDA076403

## Active ingredients

- GABAPENTIN: 250 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"17856-0600"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=17856-0600
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5969f1a8-d6d5-4967-add5-4e2492354d7b