Diclofenac Potassium
- Product NDC
- 35356-713
- 11-digit product format
- 353560713
- Labeler code
- 35356
- Product ID
- 35356-713_09e3ec78-4a4b-4c3a-996a-ea7209d56342
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA075219
- Marketing category
- ANDA
- Marketing start
- 1998-08-11
- 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 |
|---|
| 35356-713-30 | 35356071330 | 30 TABLET, FILM COATED in 1 BOTTLE (35356-713-30) | 2014-12-19 | 0000-00-00 | No | No | Current |
| 35356-713-60 | 35356071360 | 60 TABLET, FILM COATED in 1 BOTTLE (35356-713-60) | 2013-04-12 | 0000-00-00 | No | No | Current |