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
- 72189-176_5b129b3c-47a9-6d1b-e063-6394a90a810c
- Product NDC
- 72189-176
- Form
- TABLET
- Composition / generic term
- PROMETHAZINE HYDROCHLORIDE
- Labeler
- DIRECT RX
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210209
- 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 (72189-176-10) · 72189-176-10
- 12 TABLET in 1 BOTTLE (72189-176-12) · 72189-176-12
- 20 TABLET in 1 BOTTLE (72189-176-20) · 72189-176-20
- 30 TABLET in 1 BOTTLE (72189-176-30) · 72189-176-30
- 60 TABLET in 1 BOTTLE (72189-176-60) · 72189-176-60
- 90 TABLET in 1 BOTTLE (72189-176-90) · 72189-176-90
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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