Ibuprofen 43063-0872
Product NDC
43063-0872- Manufacturer
- Pd-Rx Pharmaceuticals, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 30, 2015
- Listing Expires
- December 31, 2026
- Application
- ANDA090796
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Ibuprofen | 400 mg/1 |
Drug Class
Nonsteroidal Anti-inflammatory Drug [EPC]Anti-Inflammatory AgentsNon-Steroidal [CS]
Packaging Options(7)
6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-872-06)
10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-872-10)
20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-872-20)
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-872-30)
40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-872-40)
500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-872-82)
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-872-90)