NDC 71335-0081 – Banophen

Diphenhydramine Hydrochloride 50 mg/1 · Capsule · Oral

Human Otc Drug

Product NDC71335-0081

Product details

Brand name
Banophen
Generic name
Diphenhydramine hcl
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
OTC MONOGRAPH DRUG · M012
Marketed since
November 2, 2009
Marketing end
January 31, 2028
Pharmacologic class
Histamine-1 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Banophen →

Package NDC codes (10)

Package NDCDescriptionSince
71335-0081-012 CAPSULE in 1 BOTTLE (71335-0081-0)Feb 9, 2022
71335-0081-115 CAPSULE in 1 BOTTLE (71335-0081-1)May 18, 2020
71335-0081-220 CAPSULE in 1 BOTTLE (71335-0081-2)Apr 20, 2018
71335-0081-330 CAPSULE in 1 BOTTLE (71335-0081-3)Aug 15, 2018
71335-0081-410 CAPSULE in 1 BOTTLE (71335-0081-4)Sep 9, 2019
71335-0081-56 CAPSULE in 1 BOTTLE (71335-0081-5)Aug 7, 2019
71335-0081-6100 CAPSULE in 1 BOTTLE (71335-0081-6)May 7, 2018
71335-0081-790 CAPSULE in 1 BOTTLE (71335-0081-7)Feb 9, 2022
71335-0081-860 CAPSULE in 1 BOTTLE (71335-0081-8)Feb 9, 2022
71335-0081-92 CAPSULE in 1 BOTTLE (71335-0081-9)Feb 9, 2022

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