NDC 68788-4119 – Famotidine
Famotidine 20 mg/1 · Tablet · Oral
Product NDC68788-4119
Product details
- Brand name
- Famotidine
- Generic name
- Famotidine
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA078916
- Marketed since
- June 8, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Histamine-2 Receptor Antagonist
Active ingredients
- Famotidine 20 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 68788-4119-1 | 100 TABLET in 1 BOTTLE (68788-4119-1) | Jun 8, 2026 |
| 68788-4119-3 | 30 TABLET in 1 BOTTLE (68788-4119-3) | Jun 8, 2026 |
| 68788-4119-4 | 14 TABLET in 1 BOTTLE (68788-4119-4) | Jun 8, 2026 |
| 68788-4119-6 | 60 TABLET in 1 BOTTLE (68788-4119-6) | Jun 8, 2026 |
| 68788-4119-8 | 120 TABLET in 1 BOTTLE (68788-4119-8) | Jun 8, 2026 |
| 68788-4119-9 | 90 TABLET in 1 BOTTLE (68788-4119-9) | Jun 8, 2026 |
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