NDC 68071-3420 – Famotidine
Famotidine 20 mg/1 · Tablet, Film Coated · Oral
Product NDC68071-3420
Product details
- Brand name
- Famotidine
- Generic name
- Famotidine
- Labeler
- NuCare Pharmaceuticals,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 (5)
| Package NDC | Description | Since |
|---|---|---|
| 68071-3420-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-3420-3) | Jul 26, 2023 |
| 68071-3420-6 | 60 TABLET, FILM COATED in 1 BOTTLE (68071-3420-6) | Jun 1, 2023 |
| 68071-3420-7 | 14 TABLET, FILM COATED in 1 BOTTLE (68071-3420-7) | Jul 26, 2023 |
| 68071-3420-8 | 120 TABLET, FILM COATED in 1 BOTTLE (68071-3420-8) | Jul 26, 2023 |
| 68071-3420-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68071-3420-9) | Jul 26, 2023 |
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