Oxycodone Hydrochloride 71335-0981
Generic: Oxycodone
Product NDC
71335-0981- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- October 30, 2012
- Listing Expires
- December 31, 2026
- Application
- ANDA203638
Active Ingredients
| Ingredient | Strength |
|---|---|
| Oxycodone Hydrochloride | 5 mg/1 |
Drug Class
Full Opioid Agonists [MoA]Opioid Agonist [EPC]
Packaging Options(10)
15 TABLET in 1 BOTTLE (71335-0981-0)
30 TABLET in 1 BOTTLE (71335-0981-1)
60 TABLET in 1 BOTTLE (71335-0981-2)
90 TABLET in 1 BOTTLE (71335-0981-3)
56 TABLET in 1 BOTTLE (71335-0981-4)
100 TABLET in 1 BOTTLE (71335-0981-5)
120 TABLET in 1 BOTTLE (71335-0981-6)
50 TABLET in 1 BOTTLE (71335-0981-7)
40 TABLET in 1 BOTTLE (71335-0981-8)
20 TABLET in 1 BOTTLE (71335-0981-9)