Oxycodone Hydrochloride 71335-2126
Product NDC
71335-2126- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- August 8, 2017
- Listing Expires
- December 31, 2027
- Application
- ANDA207418
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 (71335-2126-1)
90 TABLET in 1 BOTTLE (71335-2126-2)
120 TABLET in 1 BOTTLE (71335-2126-3)
30 TABLET in 1 BOTTLE (71335-2126-4)
100 TABLET in 1 BOTTLE (71335-2126-5)
40 TABLET in 1 BOTTLE (71335-2126-6)
18 TABLET in 1 BOTTLE (71335-2126-7)
28 TABLET in 1 BOTTLE (71335-2126-8)