NDC 71335-1359 – Promethazine Hydrochloride

Promethazine Hydrochloride 25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1359

Product details

Brand name
Promethazine Hydrochloride
Generic name
Promethazine hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040712
Marketed since
July 31, 2006
Listing expires
December 31, 2027
Pharmacologic class
Phenothiazine

Active ingredients

Uses, dosage, side effects and warnings for Promethazine Hydrochloride →

Package NDC codes (10)

Package NDCDescriptionSince
71335-1359-014 TABLET in 1 BOTTLE (71335-1359-0)Jul 9, 2024
71335-1359-115 TABLET in 1 BOTTLE (71335-1359-1)Mar 16, 2022
71335-1359-230 TABLET in 1 BOTTLE (71335-1359-2)Nov 26, 2019
71335-1359-310 TABLET in 1 BOTTLE (71335-1359-3)Jul 30, 2020
71335-1359-420 TABLET in 1 BOTTLE (71335-1359-4)Dec 2, 2020
71335-1359-512 TABLET in 1 BOTTLE (71335-1359-5)May 7, 2020
71335-1359-660 TABLET in 1 BOTTLE (71335-1359-6)May 12, 2020
71335-1359-790 TABLET in 1 BOTTLE (71335-1359-7)Jun 4, 2020
71335-1359-86 TABLET in 1 BOTTLE (71335-1359-8)Jan 2, 2020
71335-1359-956 TABLET in 1 BOTTLE (71335-1359-9)Sep 9, 2020

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