ibuprofen
- Product NDC
- 30142-604
- 11-digit product format
- 301420604
- Labeler code
- 30142
- Product ID
- 30142-604_205b2aed-fd65-46f8-8119-8ad76e493b1e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Kroger Company
- Application
- ANDA072096
- Marketing category
- ANDA
- Marketing start
- 1988-01-15
- 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#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 30142-604-62 | ibuprofen | 1 in 1 CARTON | TABLET, FILM COATED | 1 | | 10 |
| 30142-604-62 | ibuprofen | 24 in 1 BOTTLE | TABLET, FILM COATED | 24 | | 10 |
| 30142-604-71 | ibuprofen | 1 in 1 CARTON | TABLET, FILM COATED | 1 | | 10 |
| 30142-604-71 | ibuprofen | 50 in 1 BOTTLE | TABLET, FILM COATED | 50 | | 10 |
| 30142-604-76 | ibuprofen | 1 in 1 CARTON | TABLET, FILM COATED | 1 | | 10 |
| 30142-604-76 | ibuprofen | 120 in 1 BOTTLE | TABLET, FILM COATED | 120 | | 10 |
| 30142-604-78 | ibuprofen | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 10 |
| 30142-604-78 | ibuprofen | 1 in 1 CARTON | TABLET, FILM COATED | 1 | | 10 |
| 30142-604-85 | ibuprofen | 250 in 1 BOTTLE | TABLET, FILM COATED | 250 | | 10 |
| 30142-604-90 | ibuprofen | 500 in 1 BOTTLE | TABLET, FILM COATED | 500 | | 10 |
| 30142-604-93 | ibuprofen | 1000 in 1 BOTTLE | TABLET, FILM COATED | 1000 | | 10 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 30142-604 | IBUPROFEN TABLET, FILM COATED [KROGER COMPANY] | 9 | Current NDC, Legacy NDC, 11 package rows | 20250418_6307485a-8be6-40ee-899b-00eb3ee8ce61.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 |
|---|
| 30142-604-62 | 30142060462 | 1 BOTTLE in 1 CARTON (30142-604-62) / 24 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 1988-01-15 | 0000-00-00 | No | No | Current |
| 30142-604-71 | 30142060471 | 1 BOTTLE in 1 CARTON (30142-604-71) > 50 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 1988-02-15 | 0000-00-00 | No | No | Current |
| 30142-604-76 | 30142060476 | 1 BOTTLE in 1 CARTON (30142-604-76) > 120 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 1992-01-14 | 0000-00-00 | No | No | Current |
| 30142-604-78 | 30142060478 | 1 BOTTLE in 1 CARTON (30142-604-78) > 100 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 1988-09-15 | 0000-00-00 | No | No | Current |
| 30142-604-85 | 30142060485 | 250 TABLET, FILM COATED in 1 BOTTLE (30142-604-85) | | 2005-07-01 | 0000-00-00 | No | No | Current |
| 30142-604-90 | 30142060490 | 500 TABLET, FILM COATED in 1 BOTTLE (30142-604-90) | | 1991-11-04 | 0000-00-00 | No | No | Current |
| 30142-604-93 | 30142060493 | 1000 in 1 BOTTLE | | | | | | Historical |