DUAL ACTION BACK PAIN RELIEVER
- Product NDC
- 79481-0152
- 11-digit product format
- 794810152
- Labeler code
- 79481
- Product ID
- 79481-0152_76a6eefa-8ec6-4a1a-8aac-9fbd227e5a4d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- acetaminophen, ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Meijer, Inc.
- Application
- ANDA214836
- Marketing category
- ANDA
- Marketing start
- 2026-03-05
- 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
- 2027-12-31
- 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 |
|---|
| 79481-0152-0 | 79481015200 | 1 BOTTLE in 1 CARTON (79481-0152-0) / 72 TABLET, FILM COATED in 1 BOTTLE (79481-0152-1) | 1 bottle | 2026-03-05 | No | No | Historical |