United States · FDA National Drug Code directory
Banophen
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
- 71335-0081_6129c299-3b41-4276-a828-d074abb1669e
- Product NDC
- 71335-0081
- Form
- CAPSULE
- Composition / generic term
- diphenhydramine hcl
- Labeler
- Bryant Ranch Prepack
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20091102 / 20280131
Source-listed ingredients
- DIPHENHYDRAMINE HYDROCHLORIDE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 12 CAPSULE in 1 BOTTLE (71335-0081-0) · 71335-0081-0
- 15 CAPSULE in 1 BOTTLE (71335-0081-1) · 71335-0081-1
- 20 CAPSULE in 1 BOTTLE (71335-0081-2) · 71335-0081-2
- 30 CAPSULE in 1 BOTTLE (71335-0081-3) · 71335-0081-3
- 10 CAPSULE in 1 BOTTLE (71335-0081-4) · 71335-0081-4
- 6 CAPSULE in 1 BOTTLE (71335-0081-5) · 71335-0081-5
- 100 CAPSULE in 1 BOTTLE (71335-0081-6) · 71335-0081-6
- 90 CAPSULE in 1 BOTTLE (71335-0081-7) · 71335-0081-7
- 60 CAPSULE in 1 BOTTLE (71335-0081-8) · 71335-0081-8
- 2 CAPSULE in 1 BOTTLE (71335-0081-9) · 71335-0081-9
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →