IBUPROFEN
- Product NDC
- 50332-0152
- 11-digit product format
- 503320152
- Labeler code
- 50332
- Product ID
- 50332-0152_24531295-6ee5-4fcb-857b-50c3ea59e3c3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ibuprofen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- HART Health
- Application
- M
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-01-01
- 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
- 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 | 310965 |
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50332-0152 | IBUPROFEN TABLET [HART HEALTH] | 3 | Current NDC | 20240126_1c1374e1-890f-48ab-8f93-e84da9d5bf84.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50332-0152-4 | 50332015204 | 50 PACKET in 1 BOX, UNIT-DOSE (50332-0152-4) / 2 TABLET in 1 PACKET | 50 packet | 2023-01-01 | No | No | Historical |
| 50332-0152-7 | 50332015207 | 125 PACKET in 1 BOX, UNIT-DOSE (50332-0152-7) / 2 TABLET in 1 PACKET | 125 packet | 2023-01-01 | No | No | Historical |
| 50332-0152-8 | 50332015208 | 250 PACKET in 1 BOX, UNIT-DOSE (50332-0152-8) / 2 TABLET in 1 PACKET | 250 packet | 2023-01-01 | No | No | Historical |