up and up ibuprofen
- Product NDC
- 11673-517
- 11-digit product format
- 116730517
- Labeler code
- 11673
- Product ID
- 11673-517_9b1c7183-7ea9-4d7c-bddf-8349792116d3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Target Corporation
- Application
- ANDA077349
- Marketing category
- ANDA
- Marketing start
- 2009-06-10
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN
- Active strength
- 200 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| IBUPROFEN | ACTIVE INGREDIENT | WK2XYI10QM | UP AND UP IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [TARGET CORPORATION] | 2 | |
| IBUPROFEN | ACTIVE MOIETY | WK2XYI10QM | UP AND UP IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [TARGET CORPORATION] | 2 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | UP AND UP IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [TARGET CORPORATION] | 2 | |
| CROSCARMELLOSE SODIUM | INACTIVE INGREDIENT | M28OL1HH48 | UP AND UP IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [TARGET CORPORATION] | 2 | |
| FERRIC OXIDE RED | INACTIVE INGREDIENT | 1K09F3G675 | UP AND UP IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [TARGET CORPORATION] | 2 | |
| POLYETHYLENE GLYCOLS | INACTIVE INGREDIENT | 3WJQ0SDW1A | UP AND UP IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [TARGET CORPORATION] | 2 | |
| POLYVINYL ALCOHOL | INACTIVE INGREDIENT | 532B59J990 | UP AND UP IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [TARGET CORPORATION] | 2 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | UP AND UP IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [TARGET CORPORATION] | 2 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | UP AND UP IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [TARGET CORPORATION] | 2 | |
| STEARIC ACID | INACTIVE INGREDIENT | 4ELV7Z65AP | UP AND UP IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [TARGET CORPORATION] | 2 | |
| TALC | INACTIVE INGREDIENT | 7SEV7J4R1U | UP AND UP IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [TARGET CORPORATION] | 2 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | UP AND UP IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [TARGET CORPORATION] | 2 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11673-517 | UP AND UP IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [TARGET CORPORATION] | 5 | Legacy NDC | 20230908_ce5fe420-a0b8-4691-86f7-57fea49bd8ce.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11673-517-78 | 11673051778 | 1 BOTTLE in 1 CARTON (11673-517-78) > 100 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2009-06-10 | 0000-00-00 | No | No | Current |