NDC 80425-0589 – Famotidine
Famotidine 20 mg/1 · Tablet, Film Coated · Oral
Product NDC80425-0589
Product details
- Brand name
- Famotidine
- Generic name
- Famotidine
- Labeler
- Advanced Rx of Tennessee, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA217400
- Marketed since
- July 10, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Histamine-2 Receptor Antagonist
Active ingredients
- Famotidine 20 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 80425-0589-1 | 30 TABLET, FILM COATED in 1 BOTTLE (80425-0589-1) | Jul 10, 2026 |
| 80425-0589-2 | 60 TABLET, FILM COATED in 1 BOTTLE (80425-0589-2) | Jul 10, 2026 |
| 80425-0589-3 | 90 TABLET, FILM COATED in 1 BOTTLE (80425-0589-3) | Jul 10, 2026 |
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