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
- 43063-970_415f6daf-09f1-78a5-e063-6294a90a9553
- Product NDC
- 43063-970
- 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 — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 4 TABLET in 1 BOTTLE, PLASTIC (43063-970-04) · 43063-970-04
- 6 TABLET in 1 BOTTLE, PLASTIC (43063-970-06) · 43063-970-06
- 10 TABLET in 1 BOTTLE, PLASTIC (43063-970-10) · 43063-970-10
- 15 TABLET in 1 BOTTLE, PLASTIC (43063-970-15) · 43063-970-15
- 21 TABLET in 1 BOTTLE, PLASTIC (43063-970-21) · 43063-970-21
- 30 TABLET in 1 BOTTLE, PLASTIC (43063-970-30) · 43063-970-30
- 60 TABLET in 1 BOTTLE, PLASTIC (43063-970-60) · 43063-970-60
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →