Ibuprofen
- Product NDC
- 41250-991
- 11-digit product format
- 412500991
- Labeler code
- 41250
- Product ID
- 41250-991_45682185-18cf-431f-b4f1-842f520081b4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Meijer Distribution Inc
- Application
- ANDA075010
- Marketing category
- ANDA
- Marketing start
- 1988-05-24
- Substance
- IBUPROFEN
- Active strength
- 200 mg/1
- Pharmacologic classes
- Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Ibuprofen
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| IBUPROFEN | 200 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | WK2XYI10QM |
| Rxcui | 310965 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 41250-991-03 | Ibuprofen | 10 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 10 | | 18 |
| 41250-991-03 | Ibuprofen | 1 in 1 PACKAGE | TABLET, FILM COATED | 1 | | 18 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| IBUPROFEN | ACTIVE INGREDIENT | WK2XYI10QM | IBUPROFEN TABLET, FILM COATED [MEIJER] | 4 | |
| IBUPROFEN | ACTIVE MOIETY | WK2XYI10QM | IBUPROFEN TABLET, FILM COATED [MEIJER] | 4 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | IBUPROFEN TABLET, FILM COATED [MEIJER] | 4 | |
| FERRIC OXIDE RED | INACTIVE INGREDIENT | 1K09F3G675 | IBUPROFEN TABLET, FILM COATED [MEIJER] | 4 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | IBUPROFEN TABLET, FILM COATED [MEIJER] | 4 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | IBUPROFEN TABLET, FILM COATED [MEIJER] | 4 | |
| POLYDEXTROSE | INACTIVE INGREDIENT | VH2XOU12IE | IBUPROFEN TABLET, FILM COATED [MEIJER] | 4 | |
| POLYETHYLENE GLYCOLS | INACTIVE INGREDIENT | 3WJQ0SDW1A | IBUPROFEN TABLET, FILM COATED [MEIJER] | 4 | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | INACTIVE INGREDIENT | 5856J3G2A2 | IBUPROFEN TABLET, FILM COATED [MEIJER] | 4 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | IBUPROFEN TABLET, FILM COATED [MEIJER] | 4 | |
| STEARIC ACID | INACTIVE INGREDIENT | 4ELV7Z65AP | IBUPROFEN TABLET, FILM COATED [MEIJER] | 4 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | IBUPROFEN TABLET, FILM COATED [MEIJER] | 4 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 41250-991 | IBUPROFEN TABLET, FILM COATED [MEIJER DISTRIBUTION INC] | 16 | Current NDC, Legacy NDC, 2 package rows | 20240718_c0c64ba5-b6b0-4221-9e44-110d92c93782.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 41250-991-03 | 41250099103 | 1 BOTTLE, PLASTIC in 1 PACKAGE (41250-991-03) / 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC | 1988-05-24 | 0000-00-00 | No | No | Current |