Ibuprofen 67877-0321
Product NDC
67877-0321- Manufacturer
- Ascend Laboratories, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 21, 2015
- Listing Expires
- December 31, 2027
- Application
- ANDA091625
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Ibuprofen | 800 mg/1 |
Drug Class
Nonsteroidal Anti-inflammatory Drug [EPC]Anti-Inflammatory AgentsNon-Steroidal [CS]
Packaging Options(5)
100 TABLET, FILM COATED in 1 BOTTLE (67877-321-01)
500 TABLET, FILM COATED in 1 BOTTLE (67877-321-05)
11400 TABLET, FILM COATED in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK (67877-321-27)
30 TABLET, FILM COATED in 1 BOTTLE (67877-321-30)
50 TABLET, FILM COATED in 1 BOTTLE (67877-321-50)