OXYCODONE AND ACETAMINOPHEN
- Product NDC
- 61919-437
- 11-digit product format
- 619190437
- Labeler code
- 61919
- Product ID
- 61919-437_94e5102d-9222-52ac-e053-2995a90acf7f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- OXYCODONE AND ACETAMINOPHE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA201972
- Marketing category
- ANDA
- Marketing start
- 2018-03-12
- Marketing end
- 0000-00-00
- Substance
- OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN
- Active strength
- 10 mg/1; mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA],Opioid Agonist [EPC]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 61919-437-30 | OXYCODONE AND ACETAMINOPHEN | 30 in 1 BOTTLE | TABLET | 30 | | 4 |
| 61919-437-60 | OXYCODONE AND ACETAMINOPHEN | 60 in 1 BOTTLE | TABLET | 60 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-437 | OXYCODONE AND ACETAMINOPHEN (OXYCODONE AND ACETAMINOPHE) TABLET [DIRECT RX] | 4 | Legacy NDC, 2 package rows | 20191015_67369a20-8ff0-53d0-e053-2991aa0a58f2.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 |
|---|
| 61919-437-30 | 61919043730 | 30 TABLET in 1 BOTTLE (61919-437-30) | 30 tablet | 2018-03-12 | 0000-00-00 | No | No | Current |
| 61919-437-60 | 61919043760 | 60 TABLET in 1 BOTTLE (61919-437-60) | 60 tablet | 2018-03-12 | 0000-00-00 | No | No | Current |