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
- 63187-544_aeef8cde-a187-453e-b7fb-e179493ff427
- Product NDC
- 63187-544
- 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 — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 6 TABLET in 1 BOTTLE (63187-544-06) · 63187-544-06
- 15 TABLET in 1 BOTTLE (63187-544-15) · 63187-544-15
- 20 TABLET in 1 BOTTLE (63187-544-20) · 63187-544-20
- 30 TABLET in 1 BOTTLE (63187-544-30) · 63187-544-30
- 60 TABLET in 1 BOTTLE (63187-544-60) · 63187-544-60
- 90 TABLET in 1 BOTTLE (63187-544-90) · 63187-544-90
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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