NDC 51407-683 – Famotidine
Famotidine 20 mg/1 · Tablet · Oral
Product NDC51407-683
Product details
- Brand name
- Famotidine
- Generic name
- Famotidine
- Labeler
- Golden State Medical Supply, Inc.
- 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 (6)
| Package NDC | Description | Since |
|---|---|---|
| 51407-683-10 | 36 BOTTLE in 1 BOX (51407-683-10) / 1000 TABLET in 1 BOTTLE | Mar 8, 2023 |
| 51407-683-18 | 36 BOTTLE in 1 BOX (51407-683-18) / 180 TABLET in 1 BOTTLE | Mar 8, 2023 |
| 51407-683-25 | 36 BOTTLE in 1 BOX (51407-683-25) / 25 TABLET in 1 BOTTLE | Mar 8, 2023 |
| 51407-683-30 | 36 BOTTLE in 1 BOX (51407-683-30) / 30 TABLET in 1 BOTTLE | Mar 8, 2023 |
| 51407-683-50 | 36 BOTTLE in 1 BOX (51407-683-50) / 50 TABLET in 1 BOTTLE | Mar 8, 2023 |
| 51407-683-90 | 36 BOTTLE in 1 BOX (51407-683-90) / 90 TABLET in 1 BOTTLE | Mar 8, 2023 |
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