Diclofenac Sodium
- Product NDC
- 68071-1653
- 11-digit product format
- 680711653
- Labeler code
- 68071
- Product ID
- 68071-1653_d6ac754b-27dd-2937-e053-2995a90a2954
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac Sodium
- Dosage form
- SOLUTION
- Route
- OPHTHALMIC
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA078031
- Marketing category
- ANDA
- Marketing start
- 2008-02-14
- Marketing end
- 0000-00-00
- Substance
- DICLOFENAC SODIUM
- Active strength
- 1 mg/mL
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-1653-5 | 68071165305 | 5 mL in 1 BOTTLE (68071-1653-5) | 5 ml | 2020-01-09 | 0000-00-00 | No | No | Current |