Ibuprofen
- Product NDC
- 76413-313
- 11-digit product format
- 764130313
- Labeler code
- 76413
- Product ID
- 76413-313_593f0a32-c3b7-4af8-8a32-5d093e18e555
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Central Texas Community Health Centers
- Application
- ANDA072096
- Marketing category
- ANDA
- Marketing start
- 2003-06-24
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN
- Active strength
- 200 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 76413-313-24 | Ibuprofen | 24 in 1 BOTTLE | TABLET, FILM COATED | 24 | | 1 |
| 76413-313-24 | Ibuprofen | 1 in 1 CARTON | TABLET, FILM COATED | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76413-313 | IBUPROFEN TABLET, FILM COATED [CENTRAL TEXAS COMMUNITY HEALTH CENTERS] | 1 | Legacy NDC, 2 package rows | 20160420_2542cbee-3aca-4a2d-b9f8-07a86b0b3a43.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 76413-313-24 | 76413031324 | 24 in 1 BOTTLE | Historical |