Diclofenac Potassium
- Product NDC
- 63629-7969
- 11-digit product format
- 636297969
- Labeler code
- 63629
- Product ID
- 63629-7969_b14802ab-744c-496b-b50c-06c6f380690d
- 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 |
|---|
| 63629-7969-1 | 63629796901 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-7969-1) | 2019-03-22 | 0000-00-00 | No | No | Current |