Ibuprofen 68016-0635
Product NDC
68016-0635- Manufacturer
- Chain Drug Consortium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- March 1, 1999
- Application
- ANDA075139
Active Ingredients
| Ingredient | Strength |
|---|---|
| Ibuprofen | 200 mg/1 |
Drug Class
Nonsteroidal Anti-inflammatory Drug [EPC]Anti-Inflammatory AgentsNon-Steroidal [CS]
Packaging Options(1)
1 BOTTLE in 1 CARTON (68016-635-10) / 100 TABLET, FILM COATED in 1 BOTTLE