Oxycodone and Acetaminophen
- Product NDC
- 21695-619
- 11-digit product format
- 216950619
- Labeler code
- 21695
- Product ID
- 21695-619_0d0dbb74-4a2c-4a95-b81e-6d008cd88808
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxycodone and Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rebel Distributors Corp
- Application
- ANDA040778
- Marketing category
- ANDA
- Marketing start
- 2007-11-27
- Marketing end
- 0000-00-00
- Substance
- OXYCODONE; ACETAMINOPHEN
- Active strength
- 10 mg/1; 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 |
|---|
| 21695-619-40 | Oxycodone and Acetaminophen | 40 in 1 BOTTLE | TABLET | 40 | | 1 |
| 21695-619-60 | Oxycodone and Acetaminophen | 60 in 1 BOTTLE | TABLET | 60 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21695-619 | OXYCODONE AND ACETAMINOPHEN TABLET [REBEL DISTRIBUTORS CORP] | 1 | Legacy NDC, 2 package rows | 20110113_0d0dbb74-4a2c-4a95-b81e-6d008cd88808.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 21695-619-40 | 21695061940 | 40 in 1 BOTTLE | Historical |
| 21695-619-60 | 21695061960 | 60 in 1 BOTTLE | Historical |