# acyclovir

NDC: 68071-5100
Generic name: acyclovir
Labeler / Manufacturer: NuCare Pharmaceuticals,Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20060313
Marketing ended: 20261231
FDA application: ANDA077309

## Active ingredients

- ACYCLOVIR: 800 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68071-5100"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-5100
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=968800dc-9456-a45f-e053-2995a90aa15e