Ibuprofen
- Product NDC
- 33261-060
- 11-digit product format
- 332610060
- Labeler code
- 33261
- Product ID
- 33261-060_06f5fb33-7f65-4bc8-bbaf-be11626de267
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Aidarex Pharmaceuticals LLC
- Application
- ANDA072096
- Marketing category
- ANDA
- Marketing start
- 1994-08-16
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN
- Active strength
- 200 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 33261-060-30 | Ibuprofen | 30 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 30 | | 2 |
| 33261-060-60 | Ibuprofen | 60 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 60 | | 2 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| IBUPROFEN | ACTIVE INGREDIENT | WK2XYI10QM | IBUPROFEN TABLET, FILM COATED [AIDAREX PHARMACEUTICALS LLC] | 2 | |
| IBUPROFEN | ACTIVE MOIETY | WK2XYI10QM | IBUPROFEN TABLET, FILM COATED [AIDAREX PHARMACEUTICALS LLC] | 2 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | IBUPROFEN TABLET, FILM COATED [AIDAREX PHARMACEUTICALS LLC] | 2 | |
| CROSCARMELLOSE SODIUM | INACTIVE INGREDIENT | M28OL1HH48 | IBUPROFEN TABLET, FILM COATED [AIDAREX PHARMACEUTICALS LLC] | 2 | |
| FERRIC OXIDE RED | INACTIVE INGREDIENT | 1K09F3G675 | IBUPROFEN TABLET, FILM COATED [AIDAREX PHARMACEUTICALS LLC] | 2 | |
| FERRIC OXIDE YELLOW | INACTIVE INGREDIENT | EX438O2MRT | IBUPROFEN TABLET, FILM COATED [AIDAREX PHARMACEUTICALS LLC] | 2 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | IBUPROFEN TABLET, FILM COATED [AIDAREX PHARMACEUTICALS LLC] | 2 | |
| POLYETHYLENE GLYCOLS | INACTIVE INGREDIENT | 3WJQ0SDW1A | IBUPROFEN TABLET, FILM COATED [AIDAREX PHARMACEUTICALS LLC] | 2 | |
| POLYSORBATE 80 | INACTIVE INGREDIENT | 6OZP39ZG8H | IBUPROFEN TABLET, FILM COATED [AIDAREX PHARMACEUTICALS LLC] | 2 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | IBUPROFEN TABLET, FILM COATED [AIDAREX PHARMACEUTICALS LLC] | 2 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | IBUPROFEN TABLET, FILM COATED [AIDAREX PHARMACEUTICALS LLC] | 2 | |
| STEARIC ACID | INACTIVE INGREDIENT | 4ELV7Z65AP | IBUPROFEN TABLET, FILM COATED [AIDAREX PHARMACEUTICALS LLC] | 2 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | IBUPROFEN TABLET, FILM COATED [AIDAREX PHARMACEUTICALS LLC] | 2 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 33261-060 | IBUPROFEN TABLET, FILM COATED [AIDAREX PHARMACEUTICALS LLC] | 2 | Legacy NDC, 2 package rows | 20140110_166f18b9-b240-4af7-a6a1-029cfabfc052.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 33261-060-30 | 33261006030 | 30 in 1 BOTTLE, PLASTIC | Historical |
| 33261-060-60 | 33261006060 | 60 in 1 BOTTLE, PLASTIC | Historical |