NDC 70771-1702 – Famotidine
Famotidine 20 mg/1 · Tablet, Film Coated · Oral
Product NDC70771-1702
Product details
- Brand name
- Famotidine
- Generic name
- Famotidine
- Labeler
- Zydus Lifesciences Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA216441
- Marketed since
- June 6, 2022
- Listing expires
- December 31, 2026
- Pharmacologic class
- Histamine-2 Receptor Antagonist
Active ingredients
- Famotidine 20 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 70771-1702-0 | 1000 TABLET, FILM COATED in 1 BOTTLE (70771-1702-0) | Jun 6, 2022 |
| 70771-1702-1 | 100 TABLET, FILM COATED in 1 BOTTLE (70771-1702-1) | Jun 6, 2022 |
| 70771-1702-3 | 30 TABLET, FILM COATED in 1 BOTTLE (70771-1702-3) | Jun 6, 2022 |
| 70771-1702-4 | 10 BLISTER PACK in 1 CARTON (70771-1702-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1702-2) | Jun 6, 2022 |
| 70771-1702-5 | 500 TABLET, FILM COATED in 1 BOTTLE (70771-1702-5) | Jun 6, 2022 |
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