Diclofenac Sodium
- Product NDC
- 10544-923
- 11-digit product format
- 105440923
- Labeler code
- 10544
- Product ID
- 10544-923_7d011916-630b-4edc-9173-a70e6ad6d808
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Blenheim Pharmacal, Inc.
- Application
- ANDA074514
- Marketing category
- ANDA
- Marketing start
- 2015-05-18
- Marketing end
- 0000-00-00
- Substance
- DICLOFENAC SODIUM
- Active strength
- 50 mg/1
- Pharmacologic classes
- Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 10544-923-14 | Diclofenac Sodium | 14 in 1 BOTTLE | TABLET, DELAYED RELEASE | 14 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10544-923 | DICLOFENAC SODIUM TABLET, DELAYED RELEASE [BLENHEIM PHARMACAL, INC.] | 2 | Legacy NDC, 1 package rows | 20151029_96edaa7d-8c1c-46d1-8e80-b51072e55ed9.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 10544-923-14 | 10544092314 | 14 in 1 BOTTLE | Historical |