# Pregabalin

NDC: 55700-964
Generic name: PREGABALIN
Labeler / Manufacturer: Quality Care Products, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20220310
Marketing ended: 20270630
FDA application: ANDA208677

## Active ingredients

- PREGABALIN: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"55700-964"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55700-964
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=59432752-c8d8-4396-95dd-0e04c55bc82b