Diclofenac Sodium
- Product NDC
- 60760-154
- 11-digit product format
- 607600154
- Labeler code
- 60760
- Product ID
- 60760-154_d2450358-4a90-1a38-e053-2a95a90a32cf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA075185
- Marketing category
- ANDA
- Marketing start
- 2018-02-15
- Marketing end
- 2022-02-28
- Substance
- DICLOFENAC SODIUM
- Active strength
- 50 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
- 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 |
|---|
| 60760-154-30 | 60760015430 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-154-30) | 2018-02-15 | 0000-00-00 | No | No | Current |