NDC 80425-0422 – Ibuprofen and famotidine
Ibuprofen 800 mg/1; Famotidine 26.6 mg/1 · Tablet, Film Coated · Oral
Product NDC80425-0422
Product details
- Brand name
- Ibuprofen and famotidine
- Generic name
- Ibuprofen and famotidine
- Labeler
- Advanced Rx of Tennessee, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA211890
- Marketed since
- July 16, 2024
- 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 |
|---|---|---|
| 80425-0422-1 | 30 TABLET, FILM COATED in 1 BOTTLE (80425-0422-1) | Jul 16, 2024 |
| 80425-0422-2 | 60 TABLET, FILM COATED in 1 BOTTLE (80425-0422-2) | Jul 16, 2024 |
| 80425-0422-3 | 90 TABLET, FILM COATED in 1 BOTTLE (80425-0422-3) | Jul 16, 2024 |
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