Ibuprofen 37808-0604
Product NDC
37808-0604- Manufacturer
- H E B
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- February 15, 1989
- Listing Expires
- December 31, 2026
- Application
- ANDA072096
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 (37808-604-71) / 50 TABLET, FILM COATED in 1 BOTTLE