Diclofenac Potassium
- Product NDC
- 72789-051
- 11-digit product format
- 727890051
- Labeler code
- 72789
- Product ID
- 72789-051_e60f57c1-17f1-289a-e053-2995a90ac81d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- diclofenac potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA075463
- Marketing category
- ANDA
- Marketing start
- 1999-09-17
- Marketing end
- 2024-02-29
- Substance
- DICLOFENAC POTASSIUM
- Active strength
- 50 mg/1
- 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
- 0000-00-00
- 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 |
|---|
| 72789-051-30 | 72789005130 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-051-30) | 2021-01-18 | 0000-00-00 | No | No | Current |