Ibuprofen
- Product NDC
- 67046-308
- 11-digit product format
- 670460308
- Labeler code
- 67046
- Product ID
- 67046-308_b022458f-564e-4b5f-9541-80fadd61b733
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Contract Pharmacy Services-PA
- Application
- ANDA075682
- Marketing category
- ANDA
- Marketing start
- 2010-04-12
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN
- Active strength
- 400 mg/1
- Pharmacologic classes
- Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 67046-308-30 | Ibuprofen | 30 in 1 BLISTER PACK | TABLET | 30 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67046-308 | IBUPROFEN TABLET [CONTRACT PHARMACY SERVICES-PA] | 1 | Legacy NDC, 1 package rows | 20100415_b022458f-564e-4b5f-9541-80fadd61b733.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 67046-308-30 | 67046030830 | 30 in 1 BLISTER PACK | Historical |