Diclofenac sodium
- Product NDC
- 68001-612
- 11-digit product format
- 680010612
- Labeler code
- 68001
- Product ID
- 68001-612_3427254e-c0d3-8413-e063-6394a90a766e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- diclofenac sodium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- BluePoint Laboratories
- Application
- ANDA216275
- Marketing category
- ANDA
- Marketing start
- 2024-02-12
- Substance
- DICLOFENAC SODIUM
- Active strength
- 100 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 | 100 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | QTG126297Q |
| Rxcui | 855657 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68001-612-00 | Diclofenac sodium | 100 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 100 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68001-612 | DICLOFENAC SODIUM TABLET, FILM COATED [BLUEPOINT LABORATORIES] | 4 | Current NDC, 1 package rows | 20250503_896e3f7d-88e6-4563-b879-a2757d19fd62.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 68001-612-00 | 68001061200 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68001-612-00) | 2024-02-12 | No | No | Current |