United States · FDA National Drug Code directory
Lamivudine
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 64380-710_67507c75-76f9-490c-9366-1c2be4955d7d
- Product NDC
- 64380-710
- Form
- TABLET, FILM COATED
- Composition / generic term
- Lamivudine
- Labeler
- Strides Pharma Science Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20181019
- Source listing expiry
- 20271231
Source-listed ingredients
- LAMIVUDINE — 150 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 60 TABLET, FILM COATED in 1 BOTTLE (64380-710-03) · 64380-710-03
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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