Oxycodone HCL
- Product NDC
- 72189-618
- 11-digit product format
- 721890618
- Labeler code
- 72189
- Product ID
- 72189-618_3a851e5a-f061-4676-e063-6294a90ac16c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxycodone HCL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA077712
- Marketing category
- ANDA
- Marketing start
- 2025-04-08
- Substance
- OXYCODONE HYDROCHLORIDE
- Active strength
- 5 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 | 5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | C1ENJ2TE6C |
| Rxcui | 1049621 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72189-618-30 | Oxycodone HCL | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
| 72189-618-60 | Oxycodone HCL | 60 in 1 BOTTLE | TABLET | 60 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-618 | OXYCODONE HCL TABLET [DIRECT_RX] | 1 | Current NDC, 2 package rows | 20250410_3245cd2f-8ad0-b755-e063-6394a90a603c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72189-618-30 | 72189061830 | 30 TABLET in 1 BOTTLE (72189-618-30) | 30 tablet | 2025-04-08 | No | No | Current |
| 72189-618-60 | 72189061860 | 60 TABLET in 1 BOTTLE (72189-618-60) | 60 tablet | 2025-04-08 | No | No | Current |