NDC 63629-8891 – Ibuprofen and famotidine
Ibuprofen 800 mg/1; Famotidine 26.6 mg/1 · Tablet, Film Coated · Oral
Product NDC63629-8891
Product details
- Brand name
- Ibuprofen and famotidine
- Generic name
- Ibuprofen and famotidine
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA211890
- Marketed since
- August 4, 2021
- Listing expires
- December 31, 2026
- Pharmacologic class
- Histamine-2 Receptor Antagonist; Nonsteroidal Anti-inflammatory Drug
Active ingredients
- Ibuprofen 800 mg/1
- Famotidine 26.6 mg/1
Uses, dosage, side effects and warnings for Ibuprofen And Famotidine →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 63629-8891-1 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-8891-1) | Oct 26, 2021 |
| 63629-8891-2 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-8891-2) | Apr 8, 2022 |
| 63629-8891-3 | 60 TABLET, FILM COATED in 1 BOTTLE (63629-8891-3) | Sep 15, 2023 |
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