Oxycodone Hydrochloride
- Product NDC
- 67296-2233
- 11-digit product format
- 672962233
- Labeler code
- 67296
- Product ID
- 67296-2233_525002f7-1eab-cfdd-e063-6294a90a02c2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxycodone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Redpharm Drug
- Application
- ANDA203638
- Marketing category
- ANDA
- Marketing start
- 2012-10-30
- 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
- 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 | 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 |
|---|
| 67296-2233-2 | Oxycodone Hydrochloride | 4 in 1 BOTTLE | TABLET | 4 | | 1 |
| 67296-2233-3 | Oxycodone Hydrochloride | 6 in 1 BOTTLE | TABLET | 6 | | 1 |
| 67296-2233-7 | Oxycodone Hydrochloride | 40 in 1 BOTTLE | TABLET | 40 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 67296-2233-2 | 67296223302 | 4 TABLET in 1 BOTTLE (67296-2233-2) | 4 tablet | 2012-10-30 | No | No | Current |
| 67296-2233-3 | 67296223303 | 6 TABLET in 1 BOTTLE (67296-2233-3) | 6 tablet | 2012-10-30 | No | No | Current |
| 67296-2233-7 | 67296223307 | 40 TABLET in 1 BOTTLE (67296-2233-7) | 40 tablet | 2012-10-30 | No | No | Current |