NDC 76420-712 – Famotidine
Famotidine 20 mg/1 · Tablet, Film Coated · Oral
Product NDC76420-712
Product details
- Brand name
- Famotidine
- Generic name
- Famotidine
- Labeler
- Asclemed USA, Inc.
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 76420-712-01 | 100 TABLET, FILM COATED in 1 BOTTLE (76420-712-01) | Apr 11, 2024 |
| 76420-712-30 | 30 TABLET, FILM COATED in 1 BOTTLE (76420-712-30) | Apr 11, 2024 |
| 76420-712-60 | 60 TABLET, FILM COATED in 1 BOTTLE (76420-712-60) | Apr 11, 2024 |
| 76420-712-90 | 90 TABLET, FILM COATED in 1 BOTTLE (76420-712-90) | Apr 11, 2024 |
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