OXYCODONE/APAP
- Product NDC
- 61919-432
- 11-digit product format
- 619190432
- Labeler code
- 61919
- Product ID
- 61919-432_a7e8a9d1-15a3-7923-e053-2995a90ae440
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- OXYCODONE/APAP
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA202677
- Marketing category
- ANDA
- Marketing start
- 2016-06-15
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
- Active strength
- 325 mg/1; mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA],Opioid Agonist [EPC]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 61919-432-30 | OXYCODONE/APAP | 30 in 1 BOTTLE | TABLET | 30 | | 6 |
| 61919-432-60 | OXYCODONE/APAP | 90 in 1 BOTTLE | TABLET | 90 | | 6 |
| 61919-432-90 | OXYCODONE/APAP | 90 in 1 BOTTLE | TABLET | 90 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-432 | OXYCODONE/APAP TABLET [DIRECT RX] | 6 | Legacy NDC, 3 package rows | 20230421_355379a5-027b-3c74-e054-00144ff88e88.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 |
|---|
| 61919-432-30 | 61919043230 | 30 TABLET in 1 BOTTLE (61919-432-30) | 30 tablet | 2016-06-15 | 0000-00-00 | No | No | Current |
| 61919-432-60 | 61919043260 | 90 TABLET in 1 BOTTLE (61919-432-60) | 90 tablet | 2016-06-15 | 0000-00-00 | No | No | Current |
| 61919-432-90 | 61919043290 | 90 TABLET in 1 BOTTLE (61919-432-90) | 90 tablet | 2016-06-15 | 0000-00-00 | No | No | Current |