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
- 63187-173_0471cce6-7ddc-4530-a794-3da0d7fd94d4
- Product NDC
- 63187-173
- Form
- TABLET
- Composition / generic term
- Diazepam
- Labeler
- Proficient Rx LP
- 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
- 1 TABLET in 1 BOTTLE (63187-173-01) · 63187-173-01
- 2 TABLET in 1 BOTTLE (63187-173-02) · 63187-173-02
- 10 TABLET in 1 BOTTLE (63187-173-10) · 63187-173-10
- 15 TABLET in 1 BOTTLE (63187-173-15) · 63187-173-15
- 20 TABLET in 1 BOTTLE (63187-173-20) · 63187-173-20
- 21 TABLET in 1 BOTTLE (63187-173-21) · 63187-173-21
- 30 TABLET in 1 BOTTLE (63187-173-30) · 63187-173-30
- 60 TABLET in 1 BOTTLE (63187-173-60) · 63187-173-60
- 90 TABLET in 1 BOTTLE (63187-173-90) · 63187-173-90
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 →