NDC 71335-2126 – Oxycodone Hydrochloride
Oxycodone Hydrochloride 30 mg/1 · Tablet · Oral
Product NDC71335-2126
Product details
- Brand name
- Oxycodone Hydrochloride
- Generic name
- Oxycodone Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA207418
- Marketed since
- August 8, 2017
- Listing expires
- December 31, 2027
- 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 |
|---|---|---|
| 71335-2126-1 | 60 TABLET in 1 BOTTLE (71335-2126-1) | Jul 18, 2022 |
| 71335-2126-2 | 90 TABLET in 1 BOTTLE (71335-2126-2) | Jul 18, 2022 |
| 71335-2126-3 | 120 TABLET in 1 BOTTLE (71335-2126-3) | Jul 18, 2022 |
| 71335-2126-4 | 30 TABLET in 1 BOTTLE (71335-2126-4) | Jul 18, 2022 |
| 71335-2126-5 | 100 TABLET in 1 BOTTLE (71335-2126-5) | Jul 18, 2022 |
| 71335-2126-6 | 40 TABLET in 1 BOTTLE (71335-2126-6) | Jul 18, 2022 |
| 71335-2126-7 | 18 TABLET in 1 BOTTLE (71335-2126-7) | Jul 18, 2022 |
| 71335-2126-8 | 28 TABLET in 1 BOTTLE (71335-2126-8) | Jul 18, 2022 |
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