Oxycodone Hydrochloride
- Product NDC
- 52959-130
- 11-digit product format
- 529590130
- Labeler code
- 52959
- Product ID
- 52959-130_0438b837-f7ec-4c37-ae80-eafff9e3360b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxycodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- H.J. Harkins Company, Inc.
- Application
- ANDA091313
- Marketing category
- ANDA
- Marketing start
- 2011-02-28
- 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
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 52959-130-60 | Oxycodone Hydrochloride | 60 in 1 BOTTLE, PLASTIC | TABLET | 60 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52959-130 | OXYCODONE HYDROCHLORIDE TABLET [H.J. HARKINS COMPANY, INC.] | 3 | Legacy NDC, 1 package rows | 20111205_824f98e1-620b-41e5-8453-864bb67b4358.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 52959-130-60 | 52959013060 | 60 in 1 BOTTLE, PLASTIC | Historical |