Diclofenac Potassium
- Product NDC
- 70518-2185
- 11-digit product format
- 705182185
- Labeler code
- 70518
- Product ID
- 70518-2185_bd943e11-9a52-44dc-e053-2995a90afbfc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- diclofenac potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA075463
- Marketing category
- ANDA
- Marketing start
- 2019-07-02
- 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
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 |
|---|
| 70518-2185-0 | 70518218500 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2185-0) | 2019-07-02 | 0000-00-00 | No | No | Current |
| 70518-2185-1 | 70518218501 | 270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2185-1) | 2019-08-09 | 0000-00-00 | No | No | Current |
| 70518-2185-2 | 70518218502 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2185-2) | 2021-03-15 | 0000-00-00 | No | No | Current |