NDC 85509-1626 – Ibuprofen and famotidine
Ibuprofen 800 mg/1; Famotidine 26.6 mg/1 · Tablet, Film Coated · Oral
Product NDC85509-1626
Product details
- Brand name
- Ibuprofen and famotidine
- Generic name
- Ibuprofen and famotidine
- Labeler
- PHOENIX RX LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA211890
- Marketed since
- August 4, 2021
- Listing expires
- December 31, 2027
- 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 |
|---|---|---|
| 85509-1626-3 | 30 TABLET, FILM COATED in 1 BOTTLE (85509-1626-3) | Apr 7, 2026 |
| 85509-1626-6 | 60 TABLET, FILM COATED in 1 BOTTLE (85509-1626-6) | Apr 7, 2026 |
| 85509-1626-9 | 90 TABLET, FILM COATED in 1 BOTTLE (85509-1626-9) | Apr 7, 2026 |
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