NDC 71335-9748 – Famotidine
Famotidine 20 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-9748
Product details
- Brand name
- Famotidine
- Generic name
- Famotidine
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA215630
- Marketed since
- July 8, 2022
- Listing expires
- December 31, 2026
- Pharmacologic class
- Histamine-2 Receptor Antagonist
Active ingredients
- Famotidine 20 mg/1
Package NDC codes (9)
| Package NDC | Description | Since |
|---|---|---|
| 71335-9748-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-9748-1) | Sep 14, 2023 |
| 71335-9748-2 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-9748-2) | Oct 3, 2023 |
| 71335-9748-3 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-9748-3) | Sep 18, 2023 |
| 71335-9748-4 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-9748-4) | Sep 5, 2023 |
| 71335-9748-5 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-9748-5) | Nov 17, 2023 |
| 71335-9748-6 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-9748-6) | Apr 5, 2024 |
| 71335-9748-7 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-9748-7) | Mar 26, 2024 |
| 71335-9748-8 | 50 TABLET, FILM COATED in 1 BOTTLE (71335-9748-8) | Apr 5, 2024 |
| 71335-9748-9 | 14 TABLET, FILM COATED in 1 BOTTLE (71335-9748-9) | Apr 5, 2024 |
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