NDC 71335-0231 – Famotidine
Famotidine 40 mg/1 · Tablet · Oral
Product NDC71335-0231
Product details
- Brand name
- Famotidine
- Generic name
- Famotidine
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA078916
- Marketed since
- January 29, 2016
- Listing expires
- December 31, 2027
- Pharmacologic class
- Histamine-2 Receptor Antagonist
Active ingredients
- Famotidine 40 mg/1
Package NDC codes (8)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0231-1 | 30 TABLET in 1 BOTTLE (71335-0231-1) | Jul 26, 2018 |
| 71335-0231-2 | 60 TABLET in 1 BOTTLE (71335-0231-2) | Mar 6, 2018 |
| 71335-0231-3 | 100 TABLET in 1 BOTTLE (71335-0231-3) | Nov 11, 2019 |
| 71335-0231-4 | 90 TABLET in 1 BOTTLE (71335-0231-4) | Jul 16, 2018 |
| 71335-0231-5 | 15 TABLET in 1 BOTTLE (71335-0231-5) | Jan 31, 2019 |
| 71335-0231-6 | 120 TABLET in 1 BOTTLE (71335-0231-6) | Dec 27, 2021 |
| 71335-0231-7 | 20 TABLET in 1 BOTTLE (71335-0231-7) | Dec 27, 2021 |
| 71335-0231-8 | 10 TABLET in 1 BOTTLE (71335-0231-8) | Dec 27, 2021 |
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