Percocet
- Product NDC
- 72189-398
- 11-digit product format
- 721890398
- Labeler code
- 72189
- Product ID
- 72189-398_efe2e04f-2420-27da-e053-2a95a90a414b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxycodone/APAP
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA201278
- Marketing category
- ANDA
- Marketing start
- 2022-11-22
- 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
- 2023-12-31
- 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 |
|---|
| 72189-398-30 | Oxycodone/APAP | 30 in 1 BOTTLE | TABLET | 30 | | 4 |
| 72189-398-60 | Oxycodone/APAP | 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 |
|---|
| 72189-398 | OXYCODONE/APAP TABLET [DIRECT_RX] | 4 | Legacy NDC, 2 package rows | 20230309_ee14972b-653a-7f56-e053-2a95a90ad1be.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 |
|---|
| 72189-398-30 | 72189039830 | 30 TABLET in 1 BOTTLE (72189-398-30) | 30 tablet | 2022-11-22 | 0000-00-00 | No | No | Current |
| 72189-398-60 | 72189039860 | 60 TABLET in 1 BOTTLE (72189-398-60) | 60 tablet | 2022-11-22 | 0000-00-00 | No | No | Current |