Diclofenac sodium
- Product NDC
- 72578-092
- 11-digit product format
- 725780092
- Labeler code
- 72578
- Product ID
- 72578-092_bdebb301-fd1a-4f14-ba27-c3a0e5bfd0b1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac sodium
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Viona Pharmaceuticals Inc
- Application
- ANDA206411
- Marketing category
- ANDA
- Marketing start
- 2020-07-20
- Marketing end
- 0000-00-00
- Substance
- DICLOFENAC SODIUM
- Active strength
- 16 mg/mL
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72578-092 | DICLOFENAC SODIUM LIQUID [VIONA PHARMACEUTICALS INC] | 6 | Legacy NDC | 20241006_6b8e965f-79ca-4f48-8c02-ea44c8f1d5cf.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72578-092-01 | 72578009201 | 1 BOTTLE, DROPPER in 1 CARTON (72578-092-01) > 150 mL in 1 BOTTLE, DROPPER | 2020-07-20 | 0000-00-00 | No | No | Current |