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
- 71335-0989_1e3f0bb1-aa10-4cd0-a4a7-69999fcaf545
- Product NDC
- 71335-0989
- Form
- TABLET
- Composition / generic term
- promethazine hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20070504
- Source listing expiry
- 20271231
Source-listed ingredients
- PROMETHAZINE HYDROCHLORIDE — 12.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (71335-0989-0) · 71335-0989-0
- 12 TABLET in 1 BOTTLE (71335-0989-1) · 71335-0989-1
- 4 TABLET in 1 BOTTLE (71335-0989-2) · 71335-0989-2
- 2 TABLET in 1 BOTTLE (71335-0989-3) · 71335-0989-3
- 6 TABLET in 1 BOTTLE (71335-0989-5) · 71335-0989-5
- 10 TABLET in 1 BOTTLE (71335-0989-6) · 71335-0989-6
- 40 TABLET in 1 BOTTLE (71335-0989-7) · 71335-0989-7
- 20 TABLET in 1 BOTTLE (71335-0989-8) · 71335-0989-8
- 60 TABLET in 1 BOTTLE (71335-0989-9) · 71335-0989-9
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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