Dual Back Pain Reliever
- Product NDC
- 0363-6199
- 11-digit product format
- 003636199
- Labeler code
- 0363
- Product ID
- 0363-6199_3756a89e-f886-4dae-b5b9-896cf53166b3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- acetaminophen, ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Walgreen Company
- Application
- ANDA214836
- Marketing category
- ANDA
- Marketing start
- 2024-02-16
- Substance
- ACETAMINOPHEN; IBUPROFEN
- Active strength
- 250; 125 mg/1; mg/1
- Pharmacologic classes
- Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 362O9ITL9D | ACETAMINOPHEN | 103-90-2 | ACETAMINOPHEN |
| WK2XYI10QM | IBUPROFEN | 15687-27-1 | IBUPROFEN |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 0363-6199-23 | 00363619923 | 1 BOTTLE in 1 CARTON (0363-6199-23) / 72 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2024-02-16 | No | No | Historical |