Diclofenac Potassium
- Product NDC
- 59088-131
- 11-digit product format
- 590880131
- Labeler code
- 59088
- Product ID
- 59088-131_4a8290b8-672e-015c-e063-6394a90ad965
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac Potassium 25 mg
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- PureTek Corporation
- Application
- ANDA210078
- Marketing category
- ANDA
- Marketing start
- 2026-04-10
- Substance
- DICLOFENAC POTASSIUM
- Active strength
- 25 mg/1
- 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
- Diclofenac Potassium
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DICLOFENAC POTASSIUM | 25 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L4D5UA6CB4 |
| Rxcui | 858342 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 59088-131-73 | Diclofenac Potassium | 120 in 1 BOTTLE | CAPSULE, LIQUID FILLED | 120 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 59088-131-73 | 59088013173 | 120 CAPSULE, LIQUID FILLED in 1 BOTTLE (59088-131-73) | 2026-04-10 | No | No | Current |