NDC 72162-1335 – Oxycodone Hydrochloride
Oxycodone Hydrochloride 10 mg/1 · Tablet · Oral
Product NDC72162-1335
Product details
- Brand name
- Oxycodone Hydrochloride
- Generic name
- Oxycodone Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA091490
- Marketed since
- September 8, 2014
- Listing expires
- December 31, 2027
- Pharmacologic class
- Opioid Agonist
Active ingredients
- Oxycodone Hydrochloride 10 mg/1
Uses, dosage, side effects and warnings for Oxycodone Hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 72162-1335-2 | 120 TABLET in 1 BOTTLE (72162-1335-2) | Mar 30, 2023 |
| 72162-1335-3 | 30 TABLET in 1 BOTTLE (72162-1335-3) | Mar 30, 2023 |
| 72162-1335-6 | 60 TABLET in 1 BOTTLE (72162-1335-6) | Mar 30, 2023 |
| 72162-1335-9 | 90 TABLET in 1 BOTTLE (72162-1335-9) | Mar 30, 2023 |
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