Ibuprofen
- Product NDC
- 82501-1600
- 11-digit product format
- 825011600
- Labeler code
- 82501
- Product ID
- 82501-1600_e63dfe80-3142-4098-8407-40a875232aa8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Gobrands, Inc. (Goodnow)
- Application
- ANDA206568
- Marketing category
- ANDA
- Marketing start
- 2026-05-01
- 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
- 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 | 310964 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 82501-1600-8 | Ibuprofen | 80 in 1 BOTTLE, PLASTIC | CAPSULE, LIQUID FILLED | 80 | | 1 |
| 82501-1600-8 | Ibuprofen | 1 in 1 BOX | CAPSULE, LIQUID FILLED | 1 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 82501-1600-8 | 82501160008 | 1 BOTTLE, PLASTIC in 1 BOX (82501-1600-8) / 80 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC | 2026-05-01 | No | No | Historical |