Diclofenac Sodium
- Product NDC
- 63629-7654
- 11-digit product format
- 636297654
- Labeler code
- 63629
- Product ID
- 63629-7654_b4911440-4a28-44cf-8805-95c8ecae3b48
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075185
- Marketing category
- ANDA
- Marketing start
- 1998-11-13
- Marketing end
- 0000-00-00
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-7654-1 | 63629765401 | 800 TABLET, DELAYED RELEASE in 1 BOTTLE (63629-7654-1) | 2013-01-08 | 0000-00-00 | No | No | Current |