Oxycodone and Acetaminophen
- Product NDC
- 45865-860
- 11-digit product format
- 458650860
- Labeler code
- 45865
- Product ID
- 45865-860_20c699bc-0cef-5984-e054-00144ff88e88
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxycodone and Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Medsource Pharmaceuticals
- Application
- ANDA040777
- Marketing category
- ANDA
- Marketing start
- 2007-11-27
- Marketing end
- 0000-00-00
- Substance
- OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN
- Active strength
- 5 mg/1; 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 |
|---|
| 45865-860-40 | Oxycodone and Acetaminophen | 40 in 1 BOTTLE | TABLET | 40 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 45865-860 | OXYCODONE AND ACETAMINOPHEN TABLET [MEDSOURCE PHARMACEUTICALS] | 1 | Legacy NDC, 1 package rows | 20150928_20c699bc-0cee-5984-e054-00144ff88e88.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 45865-860-40 | 45865086040 | 40 in 1 BOTTLE | Historical |