NDC 72789-331 – Famotidine
Famotidine 20 mg/1 · Tablet, Film Coated · Oral
Product NDC72789-331
Product details
- Brand name
- Famotidine
- Generic name
- Famotidine
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA215767
- Marketed since
- November 4, 2021
- Listing expires
- December 31, 2026
- Pharmacologic class
- Histamine-2 Receptor Antagonist
Active ingredients
- Famotidine 20 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 72789-331-02 | 2 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-331-02) | Jul 30, 2024 |
| 72789-331-20 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-331-20) | Jul 10, 2023 |
| 72789-331-30 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-331-30) | Aug 1, 2023 |
| 72789-331-60 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-331-60) | Jul 28, 2023 |
| 72789-331-90 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-331-90) | Jul 17, 2023 |
| 72789-331-93 | 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-331-93) | Aug 7, 2023 |
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