IBUPROFEN
- Product NDC
- 0761-0908
- 11-digit product format
- 007610908
- Labeler code
- 0761
- Product ID
- 0761-0908_0e12b3c6-3579-b0dc-e063-6394a90a8ea4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- IBUPROFEN
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Basic Drugs, Inc.
- Application
- ANDA079174
- Marketing category
- ANDA
- Marketing start
- 2021-12-14
- 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
- Brand name suffix
- 200 MG
- 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 Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0761-0908-04 | IBUPROFEN200 MG | 250 in 1 BOTTLE | TABLET | 250 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0761-0908 | IBUPROFEN 200 MG (IBUPROFEN) TABLET [BASIC DRUGS, INC.] | 5 | Current NDC, Legacy NDC, 1 package rows | 20240104_d3351d44-2078-3adc-e053-2995a90a3c8f.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 |
|---|
| 0761-0908-04 | 00761090804 | 250 TABLET in 1 BOTTLE (0761-0908-04) | 250 tablet | 2021-12-15 | 0000-00-00 | No | No | Current |