Hydrocodone Bitartrate And Acetaminophen 27808-0035
Product NDC
27808-0035- Manufacturer
- Cranbury Pharmaceuticals, Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- October 6, 2014
- Listing Expires
- December 31, 2026
- Application
- ANDA202214
Active Ingredients
| Ingredient | Strength |
|---|---|
| Acetaminophen | 325 mg/1 |
| Hydrocodone Bitartrate | 5 mg/1 |
Drug Class
Opioid Agonist [EPC]Opioid Agonists [MoA]
Packaging Options(3)
100 TABLET in 1 BOTTLE, PLASTIC (27808-035-01)
500 TABLET in 1 BOTTLE, PLASTIC (27808-035-02)
1000 TABLET in 1 BOTTLE, PLASTIC (27808-035-03)