NDC 71335-1023 – Oxycodone Hydrochloride
Oxycodone Hydrochloride 20 mg/1 · Tablet · Oral
Product NDC71335-1023
Product details
- Brand name
- Oxycodone Hydrochloride
- Generic name
- Oxycodone
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA203638
- Marketed since
- October 30, 2012
- Listing expires
- December 31, 2026
- Pharmacologic class
- Opioid Agonist
Active ingredients
- Oxycodone Hydrochloride 20 mg/1
Uses, dosage, side effects and warnings for Oxycodone Hydrochloride →
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1023-1 | 60 TABLET in 1 BOTTLE (71335-1023-1) | Dec 7, 2018 |
| 71335-1023-2 | 90 TABLET in 1 BOTTLE (71335-1023-2) | May 30, 2024 |
| 71335-1023-3 | 28 TABLET in 1 BOTTLE (71335-1023-3) | May 30, 2024 |
| 71335-1023-4 | 30 TABLET in 1 BOTTLE (71335-1023-4) | Feb 25, 2020 |
| 71335-1023-5 | 8 TABLET in 1 BOTTLE (71335-1023-5) | May 30, 2024 |
| 71335-1023-6 | 6 TABLET in 1 BOTTLE (71335-1023-6) | May 30, 2024 |
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