NDC 83112-555 – Banophen
Diphenhydramine Hydrochloride 25 mg/1 · Tablet, Film Coated · Oral
Product NDC83112-555
Product details
- Brand name
- Banophen
- Generic name
- Diphenhydramine HCl
- Labeler
- Health Department, Oklahoma State
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketed since
- January 31, 2025
- Listing expires
- December 31, 2026
- Pharmacologic class
- Histamine-1 Receptor Antagonist
Active ingredients
- Diphenhydramine Hydrochloride 25 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 83112-555-59 | 1 TABLET, FILM COATED in 1 PACKET (83112-555-59) | Jan 31, 2025 |
Other Banophen products
- 50090-5546 Diphenhydramine Hydrochloride 25 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 63629-9451 Diphenhydramine Hydrochloride 50 mg/1 · Capsule · Bryant Ranch Prepack
- 71335-0081 Diphenhydramine Hydrochloride 50 mg/1 · Capsule · Bryant Ranch Prepack
- 0904-5307 Diphenhydramine Hydrochloride 50 mg/1 · Capsule · Major Pharmaceuticals
- 0904-5354 Diphenhydramine Hydrochloride 2 g/100g; Zinc Acetate .1 g/100g · Cream · Major Pharmaceuticals
- 0904-5551 Diphenhydramine Hydrochloride 25 mg/1 · Tablet, Film Coated · Major Pharmaceuticals
- 68788-7830 Diphenhydramine Hydrochloride 50 mg/1 · Capsule · Preferred Pharmaceuticals Inc.
- 71205-611 Diphenhydramine Hydrochloride 25 mg/1 · Tablet, Film Coated · Proficient Rx LP