Ibuprofen 200
- Product NDC
- 0363-0222
- 11-digit product format
- 003630222
- Labeler code
- 0363
- Product ID
- 0363-0222_7fc8aec2-a16c-414b-af13-f5c918052c33
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- WALGREEN COMPANY
- Application
- ANDA078682
- Marketing category
- ANDA
- Marketing start
- 2019-08-02
- 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
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Ibuprofen 200
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| IBUPROFEN | 200 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | WK2XYI10QM |
| Rxcui | 310964 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0363-0222-22 | Ibuprofen 200 | 120 in 1 BOTTLE | CAPSULE, LIQUID FILLED | 120 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0363-0222 | IBUPROFEN 200 (IBUPROFEN) CAPSULE, LIQUID FILLED [WALGREEN COMPANY] | 1 | Current NDC, Legacy NDC, 1 package rows | 20190815_5fe0bdfa-1d5b-4657-a32b-f531b69bac0d.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 |
|---|
| 0363-0222-22 | 00363022222 | 120 CAPSULE, LIQUID FILLED in 1 BOTTLE (0363-0222-22) | 2019-08-02 | 0000-00-00 | No | No | Current |