Diclofenac Potassium
- Product NDC
- 70934-906
- 11-digit product format
- 709340906
- Labeler code
- 70934
- Product ID
- 70934-906_cd898f04-084e-4c25-e053-2995a90a95ae
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- diclofenac potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA076561
- Marketing category
- ANDA
- Marketing start
- 2021-10-04
- Marketing end
- 0000-00-00
- Substance
- DICLOFENAC POTASSIUM
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-906-30 | 70934090630 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-906-30) | 2021-10-04 | 0000-00-00 | No | No | Current |