NDC 58602-829 – Famotidine
Famotidine 20 mg/1 · Tablet, Film Coated · Oral
Product NDC58602-829
Product details
- Brand name
- Famotidine
- Generic name
- Famotidine
- Labeler
- Aurohealth LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA206531
- Marketed since
- April 26, 2016
- Listing expires
- December 31, 2027
- Pharmacologic class
- Histamine-2 Receptor Antagonist
Active ingredients
- Famotidine 20 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 58602-829-21 | 1 BOTTLE in 1 CARTON (58602-829-21) / 100 TABLET, FILM COATED in 1 BOTTLE | Apr 26, 2016 |
| 58602-829-34 | 1 BOTTLE in 1 CARTON (58602-829-34) / 200 TABLET, FILM COATED in 1 BOTTLE | Mar 25, 2021 |
| 58602-829-50 | 1 BOTTLE in 1 CARTON (58602-829-50) / 85 TABLET, FILM COATED in 1 BOTTLE | Mar 2, 2021 |
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