Diclofenac Sodium
- Product NDC
- 67296-1064
- 11-digit product format
- 672961064
- Labeler code
- 67296
- Product ID
- 67296-1064_d60fb093-62d4-5fa7-e053-2995a90a3188
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA090066
- Marketing category
- ANDA
- Marketing start
- 2010-12-31
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- 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 |
|---|
| 67296-1064-1 | Diclofenac Sodium | 21 in 1 BOTTLE | TABLET, DELAYED RELEASE | 21 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1064 | DICLOFENAC SODIUM TABLET, DELAYED RELEASE [REDPHARM DRUG, INC.] | 4 | Legacy NDC, 1 package rows | 20220121_4e4112f6-0c9a-26d7-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 |
|---|
| 67296-1064-1 | 67296106401 | 21 TABLET, DELAYED RELEASE in 1 BOTTLE (67296-1064-1) | 2010-12-31 | 0000-00-00 | No | No | Current |