NDC 63629-7013 – Famotidine
Famotidine 20 mg/1 · Tablet · Oral
Product NDC63629-7013
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 (5)
| Package NDC | Description | Since |
|---|---|---|
| 63629-7013-1 | 30 TABLET in 1 BOTTLE (63629-7013-1) | Mar 14, 2005 |
| 63629-7013-2 | 60 TABLET in 1 BOTTLE (63629-7013-2) | Jun 26, 2007 |
| 63629-7013-3 | 90 TABLET in 1 BOTTLE (63629-7013-3) | Jul 16, 2007 |
| 63629-7013-4 | 10 TABLET in 1 BOTTLE (63629-7013-4) | Dec 14, 2010 |
| 63629-7013-5 | 20 TABLET in 1 BOTTLE (63629-7013-5) | Feb 4, 2013 |
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