ibuprofen
- Product NDC
- 10544-084
- 11-digit product format
- 105440084
- Labeler code
- 10544
- Product ID
- 10544-084_e702b20c-01e7-40b4-89eb-e8bd065844c0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ibuprofen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Blenheim Pharmacal, Inc.
- Application
- ANDA078329
- Marketing category
- ANDA
- Marketing start
- 2012-08-23
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN
- Active strength
- 800 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 |
|---|
| 10544-084-20 | ibuprofen | 20 in 1 BOTTLE | TABLET | 20 | | 1 |
| 10544-084-30 | ibuprofen | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10544-084 | IBUPROFEN TABLET [BLENHEIM PHARMACAL, INC.] | 1 | Legacy NDC, 2 package rows | 20151229_6316b345-beb0-4be6-a9c6-b3881d310eff.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 10544-084-20 | 10544008420 | 20 in 1 BOTTLE | Historical |
| 10544-084-30 | 10544008430 | 30 in 1 BOTTLE | Historical |