NDC 43063-695 – Famotidine
Famotidine 20 mg/1 · Tablet · Oral
Product NDC43063-695
Product details
- Brand name
- Famotidine
- Generic name
- Famotidine
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA075805
- Marketed since
- April 16, 2001
- 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 |
|---|---|---|
| 43063-695-20 | 20 TABLET in 1 BOTTLE, PLASTIC (43063-695-20) | Feb 21, 2017 |
| 43063-695-30 | 30 TABLET in 1 BOTTLE, PLASTIC (43063-695-30) | Jul 26, 2016 |
| 43063-695-60 | 60 TABLET in 1 BOTTLE, PLASTIC (43063-695-60) | Jul 26, 2016 |
| 43063-695-90 | 90 TABLET in 1 BOTTLE, PLASTIC (43063-695-90) | Jul 26, 2016 |
| 43063-695-93 | 180 TABLET in 1 BOTTLE, PLASTIC (43063-695-93) | Jul 26, 2016 |
| 43063-695-95 | 1000 TABLET in 1 BOTTLE, PLASTIC (43063-695-95) | Feb 22, 2021 |
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