Oxycodone Hydrochloride
- Product NDC
- 40032-433
- 11-digit product format
- 400320433
- Labeler code
- 40032
- Product ID
- 40032-433_ad0bb619-443b-477b-a019-77c8c6720720
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxycodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Novel Laboratories, Inc.
- Application
- ANDA204021
- Marketing category
- ANDA
- Marketing start
- 2017-06-12
- Marketing end
- 0000-00-00
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 40032-433-01 | Oxycodone Hydrochloride | 100 in 1 BOTTLE | TABLET | 100 | | 3 |
| 40032-433-03 | Oxycodone Hydrochloride | 30 in 1 BOTTLE | TABLET | 30 | | 3 |
| 40032-433-05 | Oxycodone Hydrochloride | 500 in 1 BOTTLE | TABLET | 500 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 40032-433 | OXYCODONE HYDROCHLORIDE TABLET [NOVEL LABORATORIES, INC.] | 3 | Legacy NDC, 3 package rows | 20171206_e38d98d8-3875-4bb6-8aba-d40a594205d0.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 40032-433-01 | 40032043301 | 100 in 1 BOTTLE | Historical |
| 40032-433-03 | 40032043303 | 30 in 1 BOTTLE | Historical |
| 40032-433-05 | 40032043305 | 500 in 1 BOTTLE | Historical |