DICLOFENAC SODIUM
- Product NDC
- 61919-575
- 11-digit product format
- 619190575
- Labeler code
- 61919
- Product ID
- 61919-575_9c93bba4-8e0c-74b3-e053-2995a90ad880
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DICLOFENAC SODIUM
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- DirectRX
- Application
- ANDA090066
- Marketing category
- ANDA
- Marketing start
- 2015-12-22
- 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
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 61919-575-60 | DICLOFENAC SODIUM | 60 in 1 BOTTLE | TABLET, DELAYED RELEASE | 60 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-575 | DICLOFENAC SODIUM TABLET, DELAYED RELEASE [DIRECTRX] | 2 | Legacy NDC, 1 package rows | 20200131_27f60ba8-a335-33b2-e054-00144ff8d46c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-575-60 | 61919057560 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (61919-575-60) | 2015-12-22 | 0000-00-00 | No | No | Current |