Oxycodone HCL
- Product NDC
- 72189-632
- 11-digit product format
- 721890632
- Labeler code
- 72189
- Product ID
- 72189-632_3a8579d0-8ea3-42bc-e063-6294a90a7fd2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxycodone HCL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA077712
- Marketing category
- ANDA
- Marketing start
- 2025-07-22
- Substance
- OXYCODONE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA], Opioid Agonist [EPC]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Oxycodone HCL
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| OXYCODONE HYDROCHLORIDE | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | C1ENJ2TE6C |
| Rxcui | 1049683 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72189-632-30 | Oxycodone HCL | 30 in 1 BOTTLE | TABLET | 30 | | 3 |
| 72189-632-60 | Oxycodone HCL | 60 in 1 BOTTLE | TABLET | 60 | | 3 |
| 72189-632-90 | Oxycodone HCL | 90 in 1 BOTTLE | TABLET | 90 | | 3 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72189-632-30 | 72189063230 | 30 TABLET in 1 BOTTLE (72189-632-30) | 30 tablet | 2025-07-22 | No | No | Historical |
| 72189-632-60 | 72189063260 | 60 TABLET in 1 BOTTLE (72189-632-60) | 60 tablet | 2025-07-22 | No | No | Historical |
| 72189-632-90 | 72189063290 | 90 TABLET in 1 BOTTLE (72189-632-90) | 90 tablet | 2025-07-22 | No | No | Historical |