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: 87063-015_55a50d4e-813d-b1c0-e063-6394a90a4617
Product NDC: 87063-015
Form: TABLET
Composition / generic term: Promethazine Hydrochloride
Labeler: ASCLEMED USA INC.
Marketing category: ANDA
Marketing start / end (source format): 20051214
Source listing expiry: 20271231

Source-listed ingredients

PROMETHAZINE HYDROCHLORIDE — 25 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

1000 TABLET in 1 BOTTLE (87063-015-00) · 87063-015-00
100 TABLET in 1 BOTTLE (87063-015-01) · 87063-015-01
500 TABLET in 1 BOTTLE (87063-015-05) · 87063-015-05
10 TABLET in 1 BOTTLE (87063-015-10) · 87063-015-10
12 TABLET in 1 BOTTLE (87063-015-12) · 87063-015-12
20 TABLET in 1 BOTTLE (87063-015-20) · 87063-015-20
30 TABLET in 1 BOTTLE (87063-015-30) · 87063-015-30
60 TABLET in 1 BOTTLE (87063-015-60) · 87063-015-60
90 TABLET in 1 BOTTLE (87063-015-90) · 87063-015-90

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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