Diclofenac Sodium
- Product NDC
- 68071-2045
- 11-digit product format
- 680712045
- Labeler code
- 68071
- Product ID
- 68071-2045_c01c36ac-fdfa-c84b-e053-2a95a90a3983
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA074514
- Marketing category
- ANDA
- Marketing start
- 1996-03-26
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2045-3 | 68071204503 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-2045-3) | 2018-05-09 | 0000-00-00 | No | No | Current |
| 68071-2045-6 | 68071204506 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-2045-6) | 2018-05-09 | 0000-00-00 | No | No | Current |
| 68071-2045-9 | 68071204509 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-2045-9) | 2018-05-09 | 0000-00-00 | No | No | Current |