NDC 67877-842 – Famotidine
Famotidine 20 mg/1 · Tablet, Film Coated · Oral
Product NDC67877-842
Product details
- Brand name
- Famotidine
- Generic name
- Famotidine
- Labeler
- Ascend Laboratories, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA215630
- Marketed since
- July 8, 2022
- Listing expires
- December 31, 2026
- Pharmacologic class
- Histamine-2 Receptor Antagonist
Active ingredients
- Famotidine 20 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 67877-842-01 | 100 TABLET, FILM COATED in 1 BOTTLE (67877-842-01) | Jul 8, 2022 |
| 67877-842-05 | 500 TABLET, FILM COATED in 1 BOTTLE (67877-842-05) | Feb 3, 2025 |
| 67877-842-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (67877-842-10) | Jul 8, 2022 |
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