NDC 71335-1414 – Oxycodone Hydrochloride
Oxycodone Hydrochloride 30 mg/1 · Tablet · Oral
Product NDC71335-1414
Product details
- Brand name
- Oxycodone Hydrochloride
- Generic name
- Oxycodone Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA091490
- Marketed since
- September 8, 2014
- Listing expires
- December 31, 2026
- Pharmacologic class
- Opioid Agonist
Active ingredients
- Oxycodone Hydrochloride 30 mg/1
Uses, dosage, side effects and warnings for Oxycodone Hydrochloride →
Package NDC codes (8)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1414-1 | 60 TABLET in 1 BOTTLE (71335-1414-1) | Dec 20, 2019 |
| 71335-1414-2 | 90 TABLET in 1 BOTTLE (71335-1414-2) | Dec 13, 2019 |
| 71335-1414-3 | 120 TABLET in 1 BOTTLE (71335-1414-3) | Jul 9, 2024 |
| 71335-1414-4 | 30 TABLET in 1 BOTTLE (71335-1414-4) | Dec 10, 2019 |
| 71335-1414-5 | 100 TABLET in 1 BOTTLE (71335-1414-5) | Jul 9, 2024 |
| 71335-1414-6 | 40 TABLET in 1 BOTTLE (71335-1414-6) | Jul 9, 2024 |
| 71335-1414-7 | 18 TABLET in 1 BOTTLE (71335-1414-7) | Jul 9, 2024 |
| 71335-1414-8 | 28 TABLET in 1 BOTTLE (71335-1414-8) | Jul 9, 2024 |
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