United States · FDA National Drug Code directory
PROMETHAZINE 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
- 68071-4424_57d84f2e-7c2b-08f7-e063-6394a90aa36a
- Product NDC
- 68071-4424
- Form
- TABLET
- Composition / generic term
- promethazine hydrochloride
- Labeler
- NuCare Pharmaceuticals,Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20060731
- Source listing expiry
- 20271231
Source-listed ingredients
- PROMETHAZINE HYDROCHLORIDE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TABLET in 1 BOTTLE (68071-4424-1) · 68071-4424-1
- 4 TABLET in 1 BOTTLE (68071-4424-4) · 68071-4424-4
- 6 TABLET in 1 BOTTLE (68071-4424-6) · 68071-4424-6
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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