NDC 71205-535 – Famotidine
Famotidine 20 mg/1 · Tablet, Film Coated · Oral
Product NDC71205-535
Product details
- Brand name
- Famotidine
- Generic name
- Famotidine
- Labeler
- Proficient Rx LP
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA206530
- Marketed since
- December 22, 2015
- 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 |
|---|---|---|
| 71205-535-06 | 6 TABLET, FILM COATED in 1 BOTTLE (71205-535-06) | Feb 24, 2021 |
| 71205-535-10 | 10 TABLET, FILM COATED in 1 BOTTLE (71205-535-10) | Feb 24, 2021 |
| 71205-535-30 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-535-30) | Feb 16, 2021 |
| 71205-535-60 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-535-60) | Feb 16, 2021 |
| 71205-535-78 | 180 TABLET, FILM COATED in 1 BOTTLE (71205-535-78) | Sep 6, 2024 |
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