GOODNOW PAIN RELIEF
- Product NDC
- 82501-0604
- 11-digit product format
- 825010604
- Labeler code
- 82501
- Product ID
- 82501-0604_97b525ac-bdf4-453d-91a3-eeb7f5a1f069
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Gobrands, Inc
- Application
- ANDA072096
- Marketing category
- ANDA
- Marketing start
- 2025-10-23
- 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
- GOODNOW PAIN RELIEF
- 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 |
|---|
| 82501-0604-0 | GOODNOW PAIN RELIEF | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 2 |
| 82501-0604-1 | GOODNOW PAIN RELIEF | 1 in 1 CARTON | TABLET, FILM COATED | 1 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82501-0604-0 | 82501060400 | 100 in 1 BOTTLE | | | | | Historical |
| 82501-0604-1 | 82501060401 | 1 BOTTLE in 1 CARTON (82501-0604-1) / 100 TABLET, FILM COATED in 1 BOTTLE (82501-0604-0) | 1 bottle | 2025-10-23 | No | No | Historical |