Oxycodone Hydrochloride 71335-1413
Product NDC
71335-1413- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- September 8, 2014
- Listing Expires
- December 31, 2027
- Application
- ANDA091490
Active Ingredients
| Ingredient | Strength |
|---|---|
| Oxycodone Hydrochloride | 15 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(9)
60 TABLET in 1 BOTTLE (71335-1413-1)
90 TABLET in 1 BOTTLE (71335-1413-2)
30 TABLET in 1 BOTTLE (71335-1413-3)
120 TABLET in 1 BOTTLE (71335-1413-4)
100 TABLET in 1 BOTTLE (71335-1413-5)
56 TABLET in 1 BOTTLE (71335-1413-6)
84 TABLET in 1 BOTTLE (71335-1413-7)
45 TABLET in 1 BOTTLE (71335-1413-8)
18 TABLET in 1 BOTTLE (71335-1413-9)