Diclofenac Potassium
- Product NDC
- 51655-230
- 11-digit product format
- 516550230
- Labeler code
- 51655
- Product ID
- 51655-230_48d2c42f-dd1c-d0e8-e063-6294a90a76f7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- diclofenac potassium
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Northwind Health Company, LLC
- Application
- ANDA075229
- Marketing category
- ANDA
- Marketing start
- 2022-10-27
- Substance
- DICLOFENAC POTASSIUM
- Active strength
- 50 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 | 50 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L4D5UA6CB4 |
| Rxcui | 855942 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51655-230-52 | Diclofenac Potassium | 30 in 1 BOTTLE, PLASTIC | TABLET, COATED | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51655-230 | DICLOFENAC POTASSIUM TABLET, COATED [NORTHWIND PHARMACEUTICALS, LLC] | 1 | Current NDC, 1 package rows | 20230324_f2b6a4dd-e4e2-4acc-e053-2995a90aebf2.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 51655-230-52 | 51655023052 | 30 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-230-52) | 2022-10-27 | No | No | Historical |