Ibuprofen
- Product NDC
- 11819-357
- 11-digit product format
- 118190357
- Labeler code
- 11819
- Product ID
- 11819-357_0e6315f2-49bd-471a-ab04-2949077728d0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- HHS/Program Support Center/Supply Service Center
- Application
- ANDA078558
- Marketing category
- ANDA
- Marketing start
- 2009-11-23
- 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 |
|---|
| 11819-357-40 | Ibuprofen | 40 in 1 BOTTLE, PLASTIC | TABLET | 40 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11819-357 | IBUPROFEN TABLET [HHS/PROGRAM SUPPORT CENTER/SUPPLY SERVICE CENTER] | 1 | Legacy NDC, 1 package rows | 20120314_b38fc681-6bc7-473b-b381-af0c9b42abe0.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 11819-357-40 | 11819035740 | 40 in 1 BOTTLE, PLASTIC | Historical |