Hydrocodone Bitartrate And Ibuprofen 13107-0004
Product NDC
13107-0004- Manufacturer
- Aurolife Pharma, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- June 2, 2016
- Listing Expires
- December 31, 2026
- Application
- ANDA204575
Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydrocodone Bitartrate | 7.5 mg/1 |
| Ibuprofen | 200 mg/1 |
Drug Class
Nonsteroidal Anti-inflammatory Drug [EPC]Anti-Inflammatory AgentsNon-Steroidal [CS]
Packaging Options(4)
100 TABLET, FILM COATED in 1 BOTTLE (13107-004-01)
500 TABLET, FILM COATED in 1 BOTTLE (13107-004-05)
10 TABLET, FILM COATED in 1 BOTTLE (13107-004-11)
1000 TABLET, FILM COATED in 1 BOTTLE (13107-004-99)