NDC 72865-214 – Famotidine
Famotidine 20 mg/1 · Tablet, Film Coated · Oral
Product NDC72865-214
Product details
- Brand name
- Famotidine
- Generic name
- Famotidine
- Labeler
- XLCare Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA215689
- Marketed since
- October 15, 2021
- Listing expires
- December 31, 2026
- Pharmacologic class
- Histamine-2 Receptor Antagonist
Active ingredients
- Famotidine 20 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 72865-214-01 | 100 TABLET, FILM COATED in 1 BOTTLE (72865-214-01) | Oct 15, 2021 |
| 72865-214-05 | 500 TABLET, FILM COATED in 1 BOTTLE (72865-214-05) | Oct 15, 2021 |
| 72865-214-18 | 180 TABLET, FILM COATED in 1 BOTTLE (72865-214-18) | Oct 15, 2021 |
| 72865-214-30 | 30 TABLET, FILM COATED in 1 BOTTLE (72865-214-30) | Oct 15, 2021 |
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