NDC 68788-8889 – Famotidine
Famotidine 20 mg/1 · Tablet, Film Coated · Oral
Product NDC68788-8889
Product details
- Brand name
- Famotidine
- Generic name
- Famotidine
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA075718
- Marketed since
- September 23, 2025
- Listing expires
- December 31, 2026
- Pharmacologic class
- Histamine-2 Receptor Antagonist
Active ingredients
- Famotidine 20 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 68788-8889-1 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-8889-1) | Sep 23, 2025 |
| 68788-8889-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-8889-3) | Sep 23, 2025 |
| 68788-8889-6 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-8889-6) | Sep 23, 2025 |
| 68788-8889-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-8889-9) | Sep 23, 2025 |
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