NDC 71335-0370 – Famotidine
Famotidine 20 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-0370
Product details
- Brand name
- Famotidine
- Generic name
- Famotidine
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA206530
- Marketed since
- December 22, 2015
- Listing expires
- December 31, 2026
- Pharmacologic class
- Histamine-2 Receptor Antagonist
Active ingredients
- Famotidine 20 mg/1
Package NDC codes (8)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0370-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0370-1) | Apr 16, 2021 |
| 71335-0370-2 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0370-2) | Jul 23, 2021 |
| 71335-0370-3 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-0370-3) | Dec 27, 2021 |
| 71335-0370-4 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0370-4) | May 4, 2021 |
| 71335-0370-5 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-0370-5) | Dec 27, 2021 |
| 71335-0370-6 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-0370-6) | Jun 29, 2021 |
| 71335-0370-7 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-0370-7) | Sep 2, 2021 |
| 71335-0370-8 | 50 TABLET, FILM COATED in 1 BOTTLE (71335-0370-8) | Dec 27, 2021 |
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