Diclofenac sodium
- Product NDC
- 68382-999
- 11-digit product format
- 683820999
- Labeler code
- 68382
- Product ID
- 68382-999_b048723e-cc13-4d01-bdde-c72e36a5c1af
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac sodium
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- Application
- ANDA206411
- Marketing category
- ANDA
- Marketing start
- 2018-08-08
- Marketing end
- 0000-00-00
- Substance
- DICLOFENAC SODIUM
- Active strength
- 16 mg/mL
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68382-999-01 | 68382099901 | 1 BOTTLE, DROPPER in 1 CARTON (68382-999-01) > 150 mL in 1 BOTTLE, DROPPER | 2018-08-08 | 0000-00-00 | No | No | Current |