NDC 71335-1413 – Oxycodone Hydrochloride
Oxycodone Hydrochloride 15 mg/1 · Tablet · Oral
Product NDC71335-1413
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, 2027
- Pharmacologic class
- Opioid Agonist
Active ingredients
- Oxycodone Hydrochloride 15 mg/1
Uses, dosage, side effects and warnings for Oxycodone Hydrochloride →
Package NDC codes (9)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1413-1 | 60 TABLET in 1 BOTTLE (71335-1413-1) | Feb 3, 2020 |
| 71335-1413-2 | 90 TABLET in 1 BOTTLE (71335-1413-2) | Jul 6, 2020 |
| 71335-1413-3 | 30 TABLET in 1 BOTTLE (71335-1413-3) | Mar 23, 2020 |
| 71335-1413-4 | 120 TABLET in 1 BOTTLE (71335-1413-4) | Dec 31, 2019 |
| 71335-1413-5 | 100 TABLET in 1 BOTTLE (71335-1413-5) | Jul 9, 2024 |
| 71335-1413-6 | 56 TABLET in 1 BOTTLE (71335-1413-6) | Jul 9, 2024 |
| 71335-1413-7 | 84 TABLET in 1 BOTTLE (71335-1413-7) | Jul 9, 2024 |
| 71335-1413-8 | 45 TABLET in 1 BOTTLE (71335-1413-8) | Jul 9, 2024 |
| 71335-1413-9 | 18 TABLET in 1 BOTTLE (71335-1413-9) | Jul 9, 2024 |
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