Diclofenac Sodium
- Product NDC
- 60760-058
- 11-digit product format
- 607600058
- Labeler code
- 60760
- Product ID
- 60760-058_8720ef93-26b5-0493-e053-2991aa0a8002
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac Sodium
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA076201
- Marketing category
- ANDA
- Marketing start
- 2019-04-17
- Marketing end
- 0000-00-00
- Substance
- DICLOFENAC SODIUM
- Active strength
- 100 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
- 2020-12-31
- 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 |
|---|
| 60760-058-30 | 60760005830 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-058-30) | 2019-04-17 | 0000-00-00 | No | No | Current |