Ibuprofen And Famotidine 85509-1010
Product NDC
85509-1010- Manufacturer
- Phoenix Rx Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 4, 2021
- Listing Expires
- December 31, 2026
- Application
- ANDA211890
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Famotidine | 26.6 mg/1 |
| Ibuprofen | 800 mg/1 |
Drug Class
Histamine-2 Receptor Antagonist [EPC]Nonsteroidal Anti-inflammatory Drug [EPC]Anti-Inflammatory Agents
Packaging Options(3)
30 TABLET, FILM COATED in 1 BOTTLE (85509-1010-3)
60 TABLET, FILM COATED in 1 BOTTLE (85509-1010-6)
90 TABLET, FILM COATED in 1 BOTTLE (85509-1010-9)