Ibuprofen 50844-0352
Product NDC
50844-0352- Manufacturer
- L.n.k. International, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- March 1, 1999
- Listing Expires
- December 31, 2027
- Application
- ANDA075139
Active Ingredients
| Ingredient | Strength |
|---|---|
| Ibuprofen | 200 mg/1 |
Drug Class
Nonsteroidal Anti-inflammatory Drug [EPC]Anti-Inflammatory AgentsNon-Steroidal [CS]
Packaging Options(4)
1 BOTTLE, PLASTIC in 1 CARTON (50844-352-02) / 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
1 BOTTLE, PLASTIC in 1 CARTON (50844-352-12) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
1 BOTTLE, PLASTIC in 1 CARTON (50844-352-15) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-352-16)