# PREGABALIN

NDC: 0904-7004
Generic name: PREGABALIN
Labeler / Manufacturer: Major Pharmaceuticals
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20190719

FDA application: ANDA210432

## 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:"0904-7004"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0904-7004
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2420e2d7-c01a-4590-88c5-6fe5361747e9