IBUPROFEN
- Product NDC
- 0363-0003
- 11-digit product format
- 003630003
- Labeler code
- 0363
- Product ID
- 0363-0003_5ced2456-e28d-4dc7-8255-a27b22b486b7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ibuprofen
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Walgreen Company
- Application
- ANDA079205
- Marketing category
- ANDA
- Marketing start
- 2011-05-09
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN
- Active strength
- 200 mg/1
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 0363-0003-16 | IBUPROFEN | 160 in 1 BOTTLE | CAPSULE, LIQUID FILLED | 160 | | 1 |
| 0363-0003-16 | IBUPROFEN | 1 in 1 CARTON | CAPSULE, LIQUID FILLED | 1 | | 1 |
| 0363-0003-20 | IBUPROFEN | 20 in 1 BOTTLE | CAPSULE, LIQUID FILLED | 20 | | 1 |
| 0363-0003-20 | IBUPROFEN | 1 in 1 CARTON | CAPSULE, LIQUID FILLED | 1 | | 1 |
| 0363-0003-40 | IBUPROFEN | 1 in 1 CARTON | CAPSULE, LIQUID FILLED | 1 | | 1 |
| 0363-0003-40 | IBUPROFEN | 40 in 1 BOTTLE | CAPSULE, LIQUID FILLED | 40 | | 1 |
| 0363-0003-80 | IBUPROFEN | 1 in 1 CARTON | CAPSULE, LIQUID FILLED | 1 | | 1 |
| 0363-0003-80 | IBUPROFEN | 80 in 1 BOTTLE | CAPSULE, LIQUID FILLED | 80 | | 1 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| IBUPROFEN | ACTIVE INGREDIENT | WK2XYI10QM | IBUPROFEN CAPSULE, LIQUID FILLED [WALGREEN COMPANY] | 1 | |
| IBUPROFEN | ACTIVE MOIETY | WK2XYI10QM | IBUPROFEN CAPSULE, LIQUID FILLED [WALGREEN COMPANY] | 1 | |
| AMMONIA | INACTIVE INGREDIENT | 5138Q19F1X | IBUPROFEN CAPSULE, LIQUID FILLED [WALGREEN COMPANY] | 1 | |
| FD&C GREEN NO. 3 | INACTIVE INGREDIENT | 3P3ONR6O1S | IBUPROFEN CAPSULE, LIQUID FILLED [WALGREEN COMPANY] | 1 | |
| FERROSOFERRIC OXIDE | INACTIVE INGREDIENT | XM0M87F357 | IBUPROFEN CAPSULE, LIQUID FILLED [WALGREEN COMPANY] | 1 | |
| GELATIN | INACTIVE INGREDIENT | 2G86QN327L | IBUPROFEN CAPSULE, LIQUID FILLED [WALGREEN COMPANY] | 1 | |
| MEDIUM-CHAIN TRIGLYCERIDES | INACTIVE INGREDIENT | C9H2L21V7U | IBUPROFEN CAPSULE, LIQUID FILLED [WALGREEN COMPANY] | 1 | |
| POLYETHYLENE GLYCOL | INACTIVE INGREDIENT | 3WJQ0SDW1A | IBUPROFEN CAPSULE, LIQUID FILLED [WALGREEN COMPANY] | 1 | |
| POTASSIUM HYDROXIDE | INACTIVE INGREDIENT | WZH3C48M4T | IBUPROFEN CAPSULE, LIQUID FILLED [WALGREEN COMPANY] | 1 | |
| PROPYLENE GLYCOL | INACTIVE INGREDIENT | 6DC9Q167V3 | IBUPROFEN CAPSULE, LIQUID FILLED [WALGREEN COMPANY] | 1 | |
| SHELLAC | INACTIVE INGREDIENT | 46N107B71O | IBUPROFEN CAPSULE, LIQUID FILLED [WALGREEN COMPANY] | 1 | |
| SORBITAN MONOOLEATE | INACTIVE INGREDIENT | 06XEA2VD56 | IBUPROFEN CAPSULE, LIQUID FILLED [WALGREEN COMPANY] | 1 | |
| SORBITOL | INACTIVE INGREDIENT | 506T60A25R | IBUPROFEN CAPSULE, LIQUID FILLED [WALGREEN COMPANY] | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | IBUPROFEN CAPSULE, LIQUID FILLED [WALGREEN COMPANY] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0363-0003 | IBUPROFEN CAPSULE, LIQUID FILLED [WALGREEN COMPANY] | 1 | Legacy NDC, 8 package rows | 20120618_d4569486-e581-4671-b32c-1903abfa726e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 0363-0003-16 | 00363000316 | 160 in 1 BOTTLE | Historical |
| 0363-0003-20 | 00363000320 | 20 in 1 BOTTLE | Historical |
| 0363-0003-40 | 00363000340 | 1 in 1 CARTON | Historical |
| 0363-0003-80 | 00363000380 | 1 in 1 CARTON | Historical |