OXYCODONE HYDROCHLORIDE
- Product NDC
- 68382-797
- 11-digit product format
- 683820797
- Labeler code
- 68382
- Product ID
- 68382-797_2c6f9046-4698-4b20-9d48-b89791f7f7d9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- OXYCODONE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- Application
- ANDA077290
- Marketing category
- ANDA
- Marketing start
- 2012-12-26
- Marketing end
- 0000-00-00
- Substance
- OXYCODONE HYDROCHLORIDE
- Active strength
- 30 mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA],Opioid Agonist [EPC]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 68382-797-01 | OXYCODONE HYDROCHLORIDE | 100 in 1 BOTTLE | TABLET | 100 | | 11 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68382-797 | OXYCODONE HYDROCHLORIDE TABLET [ZYDUS PHARMACEUTICALS (USA) INC. ] | 11 | Legacy NDC, 1 package rows | 20211218_86b99b2c-a270-4390-b386-496fddbb2702.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68382-797-01 | 68382079701 | 100 TABLET in 1 BOTTLE (68382-797-01) | 100 tablet | 2012-12-26 | 0000-00-00 | No | No | Current |