Ibuprofen
- Product NDC
- 68071-3679
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA202413
- Marketing category
- ANDA
- Substance
- IBUPROFEN
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 68071-3679-1 | 100 TABLET, FILM COATED in 1 BOTTLE (68071-3679-1) | 2024-09-04 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Ibuprofen Tablets, USP 400 mg, 600 mg and 800 mg | NuCare Pharmaceuticals, Inc. | 2024-09-04 | HUMAN PRESCRIPTION DRUG LABEL | 1 |