Ibuprofen
- Product NDC
- 30142-647
- 11-digit product format
- 301420647
- Labeler code
- 30142
- Product ID
- 30142-647_f8cb0ac4-b0f0-415b-bcf4-fcef3a3cab7b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Kroger Company
- Application
- ANDA072096
- Marketing category
- ANDA
- Marketing start
- 1990-10-15
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- 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 | IBUPROFEN TABLET, COATED [KROGER COMPANY] | 3 | |
| IBUPROFEN | ACTIVE MOIETY | WK2XYI10QM | IBUPROFEN TABLET, COATED [KROGER COMPANY] | 3 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | IBUPROFEN TABLET, COATED [KROGER COMPANY] | 3 | |
| CROSCARMELLOSE SODIUM | INACTIVE INGREDIENT | M28OL1HH48 | IBUPROFEN TABLET, COATED [KROGER COMPANY] | 3 | |
| FERRIC OXIDE RED | INACTIVE INGREDIENT | 1K09F3G675 | IBUPROFEN TABLET, COATED [KROGER COMPANY] | 3 | |
| FERRIC OXIDE YELLOW | INACTIVE INGREDIENT | EX438O2MRT | IBUPROFEN TABLET, COATED [KROGER COMPANY] | 3 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | IBUPROFEN TABLET, COATED [KROGER COMPANY] | 3 | |
| POLYETHYLENE GLYCOLS | INACTIVE INGREDIENT | 3WJQ0SDW1A | IBUPROFEN TABLET, COATED [KROGER COMPANY] | 3 | |
| POLYSORBATE 80 | INACTIVE INGREDIENT | 6OZP39ZG8H | IBUPROFEN TABLET, COATED [KROGER COMPANY] | 3 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | IBUPROFEN TABLET, COATED [KROGER COMPANY] | 3 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | IBUPROFEN TABLET, COATED [KROGER COMPANY] | 3 | |
| STEARIC ACID | INACTIVE INGREDIENT | 4ELV7Z65AP | IBUPROFEN TABLET, COATED [KROGER COMPANY] | 3 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | IBUPROFEN TABLET, COATED [KROGER COMPANY] | 3 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 30142-647 | IBUPROFEN TABLET, FILM COATED [KROGER COMPANY] | 6 | Legacy NDC | 20221105_ecd44ccc-f6ae-4472-a0fa-1d97f504f4cd.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 30142-647-62 | 30142064762 | 1 BOTTLE in 1 CARTON (30142-647-62) > 24 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2007-10-23 | 0000-00-00 | No | No | Current |
| 30142-647-76 | 30142064776 | 1 BOTTLE in 1 CARTON (30142-647-76) > 120 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2002-04-05 | 0000-00-00 | No | No | Current |
| 30142-647-78 | 30142064778 | 1 BOTTLE in 1 CARTON (30142-647-78) > 100 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 1994-11-04 | 0000-00-00 | No | No | Current |
| 30142-647-90 | 30142064790 | 500 TABLET, FILM COATED in 1 BOTTLE (30142-647-90) | | 2004-05-10 | 0000-00-00 | No | No | Current |