Diclofenac Potassium
- Product NDC
- 70518-3072
- 11-digit product format
- 705183072
- Labeler code
- 70518
- Product ID
- 70518-3072_debbfdaa-a864-6454-e053-2a95a90a2256
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA075219
- Marketing category
- ANDA
- Marketing start
- 2021-04-19
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- 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 |
|---|
| 70518-3072-0 | 70518307200 | 270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3072-0) | 2021-04-19 | 0000-00-00 | No | No | Current |
| 70518-3072-1 | 70518307201 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3072-1) | 2022-05-11 | 0000-00-00 | No | No | Current |