CVS Ibuprofen
- Product NDC
- 51316-187
- 11-digit product format
- 513160187
- Labeler code
- 51316
- Product ID
- 51316-187_4b0b5544-6a40-55f9-e063-6294a90a958c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- IBUPROFEN
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- CVS Pharmacy
- Application
- ANDA079129
- Marketing category
- ANDA
- Marketing start
- 2025-10-01
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- CVS Ibuprofen
- Listing expiration
- 2027-12-31
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 |
|---|
| 51316-187-00 | CVS Ibuprofen | 500 in 1 BOTTLE | TABLET | 500 | | 5 |
| 51316-187-01 | CVS Ibuprofen | 1000 in 1 BOTTLE | TABLET | 1000 | | 5 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 51316-187-00 | 51316018700 | 500 TABLET in 1 BOTTLE (51316-187-00) | 500 tablet | 2025-10-01 | No | No | Historical |
| 51316-187-01 | 51316018701 | 1000 TABLET in 1 BOTTLE (51316-187-01) | 1000 tablet | 2026-02-01 | No | No | Historical |