DICLOFENAC SODIUM
- Product NDC
- 61919-874
- 11-digit product format
- 619190874
- Labeler code
- 61919
- Product ID
- 61919-874_94e0cb71-8733-d8a5-e053-2995a90a6792
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DICLOFENAC SODIUM
- Dosage form
- SOLUTION/ DROPS
- Route
- TRANSDERMAL
- Labeler
- DIRECT RX
- Application
- ANDA204132
- Marketing category
- ANDA
- Marketing start
- 2016-09-28
- Marketing end
- 0000-00-00
- Substance
- DICLOFENAC SODIUM
- Active strength
- 16 mg/mL
- Pharmacologic classes
- Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 61919-874-05 | DICLOFENAC SODIUM | 150 mL in 1 BOTTLE | SOLUTION/ DROPS | 150 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-874 | DICLOFENAC SODIUM SOLUTION/ DROPS DICLOFENAC SODIUM SOLUTION [DIRECT RX] | 3 | Legacy NDC, 1 package rows | 20191015_3d976518-60d2-478a-e054-00144ff88e88.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-874-05 | 61919087405 | 150 mL in 1 BOTTLE (61919-874-05) | 150 ml | 2016-09-28 | 0000-00-00 | No | No | Current |