Oxycodone Hydrochloride 71335-2816
Product NDC
71335-2816- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- September 10, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA077712
Active Ingredients
| Ingredient | Strength |
|---|---|
| Oxycodone Hydrochloride | 30 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(8)
60 TABLET in 1 BOTTLE, PLASTIC (71335-2816-1)
90 TABLET in 1 BOTTLE, PLASTIC (71335-2816-2)
120 TABLET in 1 BOTTLE, PLASTIC (71335-2816-3)
30 TABLET in 1 BOTTLE, PLASTIC (71335-2816-4)
100 TABLET in 1 BOTTLE, PLASTIC (71335-2816-5)
40 TABLET in 1 BOTTLE, PLASTIC (71335-2816-6)
18 TABLET in 1 BOTTLE, PLASTIC (71335-2816-7)
28 TABLET in 1 BOTTLE, PLASTIC (71335-2816-8)