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
- 63629-1591_22f46adc-9086-4db0-8ac9-0f97914b40de
- Product NDC
- 63629-1591
- Form
- TABLET
- Composition / generic term
- Promethazine Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20051214
- Source listing expiry
- 20261231
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 (63629-1591-0) · 63629-1591-0
- 12 TABLET in 1 BOTTLE (63629-1591-1) · 63629-1591-1
- 4 TABLET in 1 BOTTLE (63629-1591-2) · 63629-1591-2
- 2 TABLET in 1 BOTTLE (63629-1591-3) · 63629-1591-3
- 6 TABLET in 1 BOTTLE (63629-1591-5) · 63629-1591-5
- 10 TABLET in 1 BOTTLE (63629-1591-6) · 63629-1591-6
- 40 TABLET in 1 BOTTLE (63629-1591-7) · 63629-1591-7
- 20 TABLET in 1 BOTTLE (63629-1591-8) · 63629-1591-8
- 60 TABLET in 1 BOTTLE (63629-1591-9) · 63629-1591-9
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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