NDC 85534-0091 – Famotidine
Famotidine 20 mg/1 · Tablet, Film Coated · Oral
Product NDC85534-0091
Product details
- Brand name
- Famotidine
- Generic name
- Famotidine
- Labeler
- HAWAII REPACK, INC.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA215630
- Marketed since
- July 8, 2022
- Listing expires
- December 31, 2027
- Pharmacologic class
- Histamine-2 Receptor Antagonist
Active ingredients
- Famotidine 20 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 85534-0091-0 | 30 TABLET, FILM COATED in 1 BOTTLE (85534-0091-0) | Jul 13, 2026 |
| 85534-0091-1 | 60 TABLET, FILM COATED in 1 BOTTLE (85534-0091-1) | Jul 13, 2026 |
| 85534-0091-2 | 90 TABLET, FILM COATED in 1 BOTTLE (85534-0091-2) | Jul 13, 2026 |
| 85534-0091-3 | 120 TABLET, FILM COATED in 1 BOTTLE (85534-0091-3) | Jul 13, 2026 |
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