Diclofenac Sodium
- Product NDC
- 72603-601
- 11-digit product format
- 726030601
- Labeler code
- 72603
- Product ID
- 72603-601_33965722-896c-cca3-e063-6394a90a3c61
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- NorthStar Rx LLC
- Application
- ANDA216548
- Marketing category
- ANDA
- Marketing start
- 2025-04-23
- Substance
- DICLOFENAC SODIUM
- 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
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Diclofenac Sodium
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DICLOFENAC SODIUM | 50 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | QTG126297Q |
| Rxcui | 855664, 855906, 855926 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72603-601-01 | Diclofenac Sodium | 1000 in 1 BOTTLE | TABLET, DELAYED RELEASE | 1000 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72603-601 | DICLOFENAC SODIUM TABLET, DELAYED RELEASE [NORTHSTAR RX LLC] | 1 | Current NDC, 1 package rows | 20250427_c7431496-c0ef-403a-9716-92d942709b3d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72603-601-01 | 72603060101 | 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (72603-601-01) | 2025-04-23 | No | No | Historical |