# Abacavir

NDC: 64980-405
Generic name: Abacavir Sulfate
Labeler / Manufacturer: Rising Pharma Holdings, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20180314

FDA application: ANDA077950

## Active ingredients

- ABACAVIR SULFATE: 20 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"64980-405"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=64980-405
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ec9e2c36-b9b7-4ac2-a366-f3ad51237f28