# Pregabalin

NDC: 76420-101
Generic name: PREGABALIN
Labeler / Manufacturer: Asclemed USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20190719

FDA application: ANDA208677

## Active ingredients

- PREGABALIN: 225 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"76420-101"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76420-101
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3d2464fb-b3ac-496e-b8a5-c2e8a902ce29