Diclofenac Sodium
- Product NDC
- 68084-333
- 11-digit product format
- 680840333
- Labeler code
- 68084
- Product ID
- 68084-333_e711fc72-71a3-550e-e053-2995a90af87d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA077863
- Marketing category
- ANDA
- Marketing start
- 2009-03-30
- Marketing end
- 2023-09-30
- Substance
- DICLOFENAC SODIUM
- Active strength
- 75 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68084-333-01 | 68084033301 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-333-01) > 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (68084-333-11) | 100 blister pack | 2009-03-30 | 0000-00-00 | No | No | Current |