Oxycodone Hydrochloride
- Product NDC
- 70166-492
- 11-digit product format
- 701660492
- Labeler code
- 70166
- Product ID
- 70166-492_615dce0a-f783-5067-e053-2a91aa0aca6e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxycodone Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Lohxa
- Application
- ANDA204092
- Marketing category
- ANDA
- Marketing start
- 2017-12-27
- Marketing end
- 0000-00-00
- Substance
- OXYCODONE HYDROCHLORIDE
- Active strength
- 100 mg/5mL
- 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 |
|---|
| 70166-492-10 | Oxycodone Hydrochloride | 30 in 1 CARTON | SOLUTION | 30 | | 1 |
| 70166-492-10 | Oxycodone Hydrochloride | 1 in 1 BAG | SOLUTION | 1 | | 1 |
| 70166-492-20 | Oxycodone Hydrochloride | 30 in 1 CARTON | SOLUTION | 30 | | 1 |
| 70166-492-20 | Oxycodone Hydrochloride | 1 in 1 BAG | SOLUTION | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70166-492 | OXYCODONE HYDROCHLORIDE SOLUTION [LOHXA] | 1 | Legacy NDC, 4 package rows | 20180126_2d5477df-9bd0-49df-a366-67b8f2817ee2.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 70166-492-10 | 70166049210 | 30 in 1 CARTON | Historical |
| 70166-492-20 | 70166049220 | 30 in 1 CARTON | Historical |