IBUPROFEN
- Product NDC
- 67060-750
- 11-digit product format
- 670600750
- Labeler code
- 67060
- Product ID
- 67060-750_93db533b-4cd4-43c3-ba68-0c627b9446af
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- IBUPROFEN 200MG
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- ADVANCED FIRST AID, INC.
- Application
- ANDA079129
- Marketing category
- ANDA
- Marketing start
- 2015-04-09
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN
- Active strength
- 200 1/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 67060-750-67 | IBUPROFEN | 250 in 1 CARTON | TABLET, FILM COATED | 250 | | 2 |
| 67060-750-67 | IBUPROFEN | 2 in 1 PACKET | TABLET, FILM COATED | 2 | | 2 |
| 67060-750-68 | IBUPROFEN | 100 in 1 CARTON | TABLET, FILM COATED | 100 | | 2 |
| 67060-750-68 | IBUPROFEN | 2 in 1 PACKET | TABLET, FILM COATED | 2 | | 2 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| IBUPROFEN | ACTIVE INGREDIENT | WK2XYI10QM | IBUPROFEN (IBUPROFEN 200MG) TABLET, FILM COATED [ADVANCED FIRST AID, INC.] | 1 | |
| IBUPROFEN | ACTIVE MOIETY | WK2XYI10QM | IBUPROFEN (IBUPROFEN 200MG) TABLET, FILM COATED [ADVANCED FIRST AID, INC.] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | IBUPROFEN (IBUPROFEN 200MG) TABLET, FILM COATED [ADVANCED FIRST AID, INC.] | 1 | |
| COLLOIDAL SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | IBUPROFEN (IBUPROFEN 200MG) TABLET, FILM COATED [ADVANCED FIRST AID, INC.] | 1 | |
| CROSCARMELLOSE SODIUM | INACTIVE INGREDIENT | M28OL1HH48 | IBUPROFEN (IBUPROFEN 200MG) TABLET, FILM COATED [ADVANCED FIRST AID, INC.] | 1 | |
| FERRIC OXIDE RED | INACTIVE INGREDIENT | 1K09F3G675 | IBUPROFEN (IBUPROFEN 200MG) TABLET, FILM COATED [ADVANCED FIRST AID, INC.] | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | IBUPROFEN (IBUPROFEN 200MG) TABLET, FILM COATED [ADVANCED FIRST AID, INC.] | 1 | |
| POLYETHYLENE GLYCOL 400 | INACTIVE INGREDIENT | B697894SGQ | IBUPROFEN (IBUPROFEN 200MG) TABLET, FILM COATED [ADVANCED FIRST AID, INC.] | 1 | |
| POLYVINYL ALCOHOL | INACTIVE INGREDIENT | 532B59J990 | IBUPROFEN (IBUPROFEN 200MG) TABLET, FILM COATED [ADVANCED FIRST AID, INC.] | 1 | |
| STARCH, PREGELATINIZED CORN | INACTIVE INGREDIENT | O8232NY3SJ | IBUPROFEN (IBUPROFEN 200MG) TABLET, FILM COATED [ADVANCED FIRST AID, INC.] | 1 | |
| TALC | INACTIVE INGREDIENT | 7SEV7J4R1U | IBUPROFEN (IBUPROFEN 200MG) TABLET, FILM COATED [ADVANCED FIRST AID, INC.] | 1 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | IBUPROFEN (IBUPROFEN 200MG) TABLET, FILM COATED [ADVANCED FIRST AID, INC.] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67060-750 | IBUPROFEN (IBUPROFEN 200MG) TABLET, FILM COATED [ADVANCED FIRST AID, INC.] | 2 | Legacy NDC, 4 package rows | 20191002_eb0e3dcf-3c99-4c6e-b133-4299d855141b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67060-750-67 | 67060075067 | 250 PACKET in 1 CARTON (67060-750-67) > 2 TABLET, FILM COATED in 1 PACKET | 250 packet | 2015-04-09 | 0000-00-00 | No | No | Current |
| 67060-750-68 | 67060075068 | 100 PACKET in 1 CARTON (67060-750-68) > 2 TABLET, FILM COATED in 1 PACKET | 100 packet | 2015-04-09 | 0000-00-00 | No | No | Current |