NDC 71335-2816 – Oxycodone Hydrochloride
Oxycodone Hydrochloride 30 mg/1 · Tablet · Oral
Product NDC71335-2816
Product details
- Brand name
- Oxycodone Hydrochloride
- Generic name
- Oxycodone Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA077712
- Marketed since
- September 10, 2024
- 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 |
|---|---|---|
| 71335-2816-1 | 60 TABLET in 1 BOTTLE, PLASTIC (71335-2816-1) | Oct 16, 2025 |
| 71335-2816-2 | 90 TABLET in 1 BOTTLE, PLASTIC (71335-2816-2) | Oct 16, 2025 |
| 71335-2816-3 | 120 TABLET in 1 BOTTLE, PLASTIC (71335-2816-3) | Oct 16, 2025 |
| 71335-2816-4 | 30 TABLET in 1 BOTTLE, PLASTIC (71335-2816-4) | Oct 16, 2025 |
| 71335-2816-5 | 100 TABLET in 1 BOTTLE, PLASTIC (71335-2816-5) | Oct 16, 2025 |
| 71335-2816-6 | 40 TABLET in 1 BOTTLE, PLASTIC (71335-2816-6) | Oct 16, 2025 |
| 71335-2816-7 | 18 TABLET in 1 BOTTLE, PLASTIC (71335-2816-7) | Oct 16, 2025 |
| 71335-2816-8 | 28 TABLET in 1 BOTTLE, PLASTIC (71335-2816-8) | Oct 16, 2025 |
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- 65162-048 Oxycodone Hydrochloride 10 mg/1 · Tablet · Amneal Pharmaceuticals LLC
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