Oxycodone Hydrochloride
- Product NDC
- 31722-486
- 11-digit product format
- 317220486
- Labeler code
- 31722
- Product ID
- 31722-486_a506a2bf-6041-4ed7-bf7c-ffe50b1b3c2e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxycodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Camber Pharmaceuticals Inc
- Application
- ANDA207418
- Marketing category
- ANDA
- Marketing start
- 2025-11-14
- Substance
- OXYCODONE HYDROCHLORIDE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA], Opioid Agonist [EPC]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Oxycodone Hydrochloride
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| OXYCODONE HYDROCHLORIDE | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | C1ENJ2TE6C |
| Rxcui | 1049611, 1049618, 1049621, 1049683, 1049686 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 31722-486-01 | 31722048601 | 100 TABLET in 1 BOTTLE (31722-486-01) | 100 tablet | 2025-11-14 | No | No | Historical |
| 31722-486-05 | 31722048605 | 500 TABLET in 1 BOTTLE (31722-486-05) | 500 tablet | 2025-11-14 | No | No | Historical |