NDC 71335-0981 – Oxycodone Hydrochloride
Oxycodone Hydrochloride 5 mg/1 · Tablet · Oral
Product NDC71335-0981
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 5 mg/1
Uses, dosage, side effects and warnings for Oxycodone Hydrochloride →
Package NDC codes (10)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0981-0 | 15 TABLET in 1 BOTTLE (71335-0981-0) | May 30, 2024 |
| 71335-0981-1 | 30 TABLET in 1 BOTTLE (71335-0981-1) | Nov 29, 2018 |
| 71335-0981-2 | 60 TABLET in 1 BOTTLE (71335-0981-2) | Nov 8, 2018 |
| 71335-0981-3 | 90 TABLET in 1 BOTTLE (71335-0981-3) | Nov 30, 2018 |
| 71335-0981-4 | 56 TABLET in 1 BOTTLE (71335-0981-4) | May 30, 2024 |
| 71335-0981-5 | 100 TABLET in 1 BOTTLE (71335-0981-5) | May 30, 2024 |
| 71335-0981-6 | 120 TABLET in 1 BOTTLE (71335-0981-6) | May 30, 2024 |
| 71335-0981-7 | 50 TABLET in 1 BOTTLE (71335-0981-7) | May 30, 2024 |
| 71335-0981-8 | 40 TABLET in 1 BOTTLE (71335-0981-8) | May 30, 2024 |
| 71335-0981-9 | 20 TABLET in 1 BOTTLE (71335-0981-9) | Oct 29, 2018 |
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