NDC 68071-3201 – Famotidine
Famotidine 20 mg/1 · Tablet · Oral
Product NDC68071-3201
Product details
- Brand name
- Famotidine
- Generic name
- Famotidine
- Labeler
- NuCare Pharmaceuticals, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA078916
- Marketed since
- January 29, 2016
- 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 |
|---|---|---|
| 68071-3201-2 | 20 TABLET in 1 BOTTLE (68071-3201-2) | Mar 24, 2017 |
| 68071-3201-3 | 30 TABLET in 1 BOTTLE (68071-3201-3) | Mar 24, 2017 |
| 68071-3201-6 | 60 TABLET in 1 BOTTLE (68071-3201-6) | Mar 24, 2017 |
| 68071-3201-8 | 180 TABLET in 1 BOTTLE (68071-3201-8) | Mar 24, 2017 |
| 68071-3201-9 | 90 TABLET in 1 BOTTLE (68071-3201-9) | Mar 24, 2017 |
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