Diclofenac Sodium
- Product NDC
- 51021-150
- 11-digit product format
- 510210150
- Labeler code
- 51021
- Product ID
- 51021-150_7d4f42aa-5036-2484-e053-2991aa0ad9c4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac Sodium
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Sircle Laboratories, LLC
- Application
- ANDA202769
- Marketing category
- ANDA
- Marketing start
- 2015-07-08
- Marketing end
- 0000-00-00
- Substance
- DICLOFENAC SODIUM
- Active strength
- 16 mg/mL
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record