United States · FDA National Drug Code directory
Diazepam
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
- 43063-987_415f8162-1d01-9092-e063-6394a90ace01
- Product NDC
- 43063-987
- Form
- TABLET
- Composition / generic term
- Diazepam
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19861210
- Source listing expiry
- 20261231
Source-listed ingredients
- DIAZEPAM — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 2 TABLET in 1 BOTTLE, PLASTIC (43063-987-02) · 43063-987-02
- 20 TABLET in 1 BOTTLE, PLASTIC (43063-987-20) · 43063-987-20
- 30 TABLET in 1 BOTTLE, PLASTIC (43063-987-30) · 43063-987-30
- 60 TABLET in 1 BOTTLE, PLASTIC (43063-987-60) · 43063-987-60
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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