Diclofenac Sodium
- Product NDC
- 70882-115
- 11-digit product format
- 708820115
- Labeler code
- 70882
- Product ID
- 70882-115_2463e68f-4f8c-4334-a45e-8204a53d9f83
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Cambridge Therapeutics Technologies, LLC
- Application
- ANDA074394
- Marketing category
- ANDA
- Marketing start
- 1995-11-30
- Marketing end
- 0000-00-00
- Substance
- DICLOFENAC SODIUM
- Active strength
- 75 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
- 2019-12-31
- 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 |
|---|
| 70882-115-30 | Diclofenac Sodium | 30 in 1 BLISTER PACK | TABLET, DELAYED RELEASE | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70882-115 | DICLOFENAC SODIUM TABLET, DELAYED RELEASE [CAMBRIDGE THERAPEUTICS TECHNOLOGIES, LLC] | 1 | Legacy NDC, 1 package rows | 20161217_a5708cc2-d9b6-428c-86df-5dbbd4a6b311.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 70882-115-30 | 70882011530 | 30 in 1 BLISTER PACK | Historical |