United States · FDA National Drug Code directory
CHLORDIAZEPOXIDE HYDROCHLORIDE
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
- 42806-562_eab706f9-1c3b-4be4-a118-4cfd55ce2c11
- Product NDC
- 42806-562
- Form
- CAPSULE, GELATIN COATED
- Composition / generic term
- CHLORDIAZEPOXIDE HYDROCHLORIDE
- Labeler
- Epic Pharma LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210511
- Source listing expiry
- 20261231
Source-listed ingredients
- CHLORDIAZEPOXIDE HYDROCHLORIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE, GELATIN COATED in 1 BOTTLE (42806-562-01) · 42806-562-01
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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