NDC 71335-1520 – Famotidine
Famotidine 20 mg/1 · Tablet · Oral
Product NDC71335-1520
Product details
- Brand name
- Famotidine
- Generic name
- Famotidine
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA075805
- Marketed since
- April 16, 2001
- 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 |
|---|---|---|
| 71335-1520-1 | 30 TABLET in 1 BOTTLE (71335-1520-1) | Feb 20, 2020 |
| 71335-1520-2 | 60 TABLET in 1 BOTTLE (71335-1520-2) | Mar 30, 2021 |
| 71335-1520-3 | 20 TABLET in 1 BOTTLE (71335-1520-3) | Jul 14, 2022 |
| 71335-1520-4 | 90 TABLET in 1 BOTTLE (71335-1520-4) | Feb 15, 2022 |
| 71335-1520-5 | 100 TABLET in 1 BOTTLE (71335-1520-5) | Sep 6, 2024 |
| 71335-1520-6 | 10 TABLET in 1 BOTTLE (71335-1520-6) | Jun 29, 2021 |
| 71335-1520-7 | 120 TABLET in 1 BOTTLE (71335-1520-7) | Oct 7, 2021 |
| 71335-1520-8 | 50 TABLET in 1 BOTTLE (71335-1520-8) | Sep 6, 2024 |
| 71335-1520-9 | 14 TABLET in 1 BOTTLE (71335-1520-9) | Sep 6, 2024 |
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