NDC 71335-0677 – Oxycodone Hydrochloride
Oxycodone Hydrochloride 30 mg/1 · Tablet · Oral
Product NDC71335-0677
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 30 mg/1
Uses, dosage, side effects and warnings for Oxycodone Hydrochloride →
Package NDC codes (8)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0677-1 | 60 TABLET in 1 BOTTLE (71335-0677-1) | Mar 9, 2018 |
| 71335-0677-2 | 90 TABLET in 1 BOTTLE (71335-0677-2) | Feb 27, 2018 |
| 71335-0677-3 | 120 TABLET in 1 BOTTLE (71335-0677-3) | May 24, 2018 |
| 71335-0677-4 | 30 TABLET in 1 BOTTLE (71335-0677-4) | Apr 30, 2018 |
| 71335-0677-5 | 100 TABLET in 1 BOTTLE (71335-0677-5) | May 29, 2024 |
| 71335-0677-6 | 40 TABLET in 1 BOTTLE (71335-0677-6) | May 29, 2024 |
| 71335-0677-7 | 18 TABLET in 1 BOTTLE (71335-0677-7) | May 29, 2024 |
| 71335-0677-8 | 28 TABLET in 1 BOTTLE (71335-0677-8) | May 29, 2024 |
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