Oxycodone and Acetaminophen
- Product NDC
- 72022-582
- 11-digit product format
- 720220582
- Labeler code
- 72022
- Product ID
- 72022-582_18d97a2f-5cfe-8079-d83a-fab6168026f6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxycodone and Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Halo Pharmaceutical Inc
- Application
- ANDA207834
- Marketing category
- ANDA
- Marketing start
- 2020-02-15
- 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
- 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 |
|---|
| 72022-582-01 | Oxycodone and Acetaminophen | 100 in 1 BOTTLE | TABLET | 100 | | 3 |
| 72022-582-05 | Oxycodone and Acetaminophen | 500 in 1 BOTTLE | TABLET | 500 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72022-582 | OXYCODONE AND ACETAMINOPHEN TABLET [HALO PHARMACEUTICAL INC] | 3 | Legacy NDC, 2 package rows | 20200215_e648ccbd-a8bb-ecfe-1bc9-7b99d33152e1.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 72022-582-01 | 72022058201 | 100 in 1 BOTTLE | Historical |
| 72022-582-05 | 72022058205 | 500 in 1 BOTTLE | Historical |