Diclofenac Potassium
- Product NDC
- 71335-0369
- 11-digit product format
- 713350369
- Labeler code
- 71335
- Product ID
- 71335-0369_f845fac9-5ca8-40e5-b316-a748508380e6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- diclofenac potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075463
- Marketing category
- ANDA
- Marketing start
- 1999-09-17
- Marketing end
- 2023-01-31
- 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 |
|---|
| 71335-0369-1 | 71335036901 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-0369-1) | 2017-07-03 | 0000-00-00 | No | No | Current |
| 71335-0369-2 | 71335036902 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0369-2) | 2017-07-03 | 0000-00-00 | No | No | Current |
| 71335-0369-3 | 71335036903 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0369-3) | 2017-07-03 | 0000-00-00 | No | No | Current |
| 71335-0369-4 | 71335036904 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0369-4) | 2017-07-03 | 0000-00-00 | No | No | Current |
| 71335-0369-5 | 71335036905 | 45 TABLET, FILM COATED in 1 BOTTLE (71335-0369-5) | 2017-07-03 | 0000-00-00 | No | No | Current |
| 71335-0369-6 | 71335036906 | 58 TABLET, FILM COATED in 1 BOTTLE (71335-0369-6) | 2017-07-03 | 0000-00-00 | No | No | Current |
| 71335-0369-7 | 71335036907 | 18 TABLET, FILM COATED in 1 BOTTLE (71335-0369-7) | 2017-07-03 | 0000-00-00 | No | No | Current |
| 71335-0369-8 | 71335036908 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-0369-8) | 2017-07-03 | 0000-00-00 | No | No | Current |