NDC 80425-0329 – Famotidine
Famotidine 20 mg/1 · Tablet, Film Coated · Oral
Product NDC80425-0329
Product details
- Brand name
- Famotidine
- Generic name
- Famotidine
- Labeler
- Advanced Rx Pharmacy of Tennessee, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA215767
- Marketed since
- April 24, 2023
- Listing expires
- December 31, 2026
- Pharmacologic class
- Histamine-2 Receptor Antagonist
Active ingredients
- Famotidine 20 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 80425-0329-1 | 30 TABLET, FILM COATED in 1 BOTTLE (80425-0329-1) | Apr 24, 2023 |
| 80425-0329-2 | 60 TABLET, FILM COATED in 1 BOTTLE (80425-0329-2) | Apr 24, 2023 |
| 80425-0329-3 | 90 TABLET, FILM COATED in 1 BOTTLE (80425-0329-3) | Apr 24, 2023 |
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