good sense ibuprofen
- Product NDC
- 50090-7053
- 11-digit product format
- 500907053
- Labeler code
- 50090
- Product ID
- 50090-7053_3830ebca-3430-4874-9ab8-5b2608bb73d5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA072096
- Marketing category
- ANDA
- Marketing start
- 1991-02-15
- Substance
- IBUPROFEN
- Active strength
- 200 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 |
|---|
| WK2XYI10QM | IBUPROFEN | 15687-27-1 | IBUPROFEN |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7053-0 | 50090705300 | 50 TABLET, FILM COATED in 1 BOTTLE (50090-7053-0) | 2024-01-15 | No | No | Historical |
| 50090-7053-3 | 50090705303 | 24 TABLET, FILM COATED in 1 BOTTLE (50090-7053-3) | 2024-01-15 | No | No | Historical |
| 50090-7053-8 | 50090705308 | 100 TABLET, FILM COATED in 1 BOTTLE (50090-7053-8) | 2024-01-15 | No | No | Historical |