HYDROCODONE BITARTRATE AND IBUPROFEN
- Product NDC
- 67296-1282
- 11-digit product format
- 672961282
- Labeler code
- 67296
- Product ID
- 67296-1282_9c9f4448-d92b-9258-e053-2a95a90a532f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- HYDROCODONE BITARTRATE AND IBUPROFEN
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA076604
- Marketing category
- ANDA
- Marketing start
- 2004-04-01
- Marketing end
- 0000-00-00
- Substance
- HYDROCODONE BITARTRATE; IBUPROFEN
- Active strength
- 8 mg/1; mg/1
- Pharmacologic classes
- Opioid Agonist [EPC],Opioid Agonists [MoA],Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [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 |
|---|
| 67296-1282-5 | HYDROCODONE BITARTRATE AND IBUPROFEN | 15 in 1 BOTTLE | TABLET, FILM COATED | 15 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1282 | HYDROCODONE BITARTRATE AND IBUPROFEN TABLET, FILM COATED [REDPHARM DRUG, INC.] | 2 | Legacy NDC, 1 package rows | 20200121_4fbc673b-546a-4845-e054-00144ff88e88.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67296-1282-5 | 67296128205 | 15 TABLET, FILM COATED in 1 BOTTLE (67296-1282-5) | 2004-04-01 | 0000-00-00 | No | No | Current |