arthritis pain reliever
- Product NDC
- 42507-150
- 11-digit product format
- 425070150
- Labeler code
- 42507
- Product ID
- 42507-150_3b7c4072-d4f5-448d-bc10-c9768fd884f5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- DICLOFENAC SODIUM
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- HyVee Inc
- Application
- ANDA211253
- Marketing category
- ANDA
- Marketing start
- 2026-04-23
- Substance
- DICLOFENAC SODIUM
- Active strength
- 10 mg/g
- Pharmacologic classes
- Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Prostaglandin Production [PE], 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
- arthritis pain reliever
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DICLOFENAC SODIUM | 10 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | QTG126297Q |
| Rxcui | 855633 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 42507-150-00 | arthritis pain reliever | 100 g in 1 TUBE | GEL | 100 | | 2 |
| 42507-150-01 | arthritis pain reliever | 1 in 1 CARTON | GEL | 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 |
|---|
| 42507-150-00 | 42507015000 | 100 g in 1 TUBE | 100 g | | | | Historical |
| 42507-150-01 | 42507015001 | 1 TUBE in 1 CARTON (42507-150-01) / 100 g in 1 TUBE (42507-150-00) | 1 tube | 2026-04-23 | No | No | Current |