Diclofenac sodium
- Product NDC
- 70771-1415
- 11-digit product format
- 707711415
- Labeler code
- 70771
- Product ID
- 70771-1415_6fe4198f-ff6e-4805-a8a6-57061f6d57cf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac sodium
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Zydus Lifesciences Limited
- 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
- 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 |
|---|
| 70771-1415 | DICLOFENAC SODIUM LIQUID [ZYDUS LIFESCIENCES LIMITED] | 5 | Legacy NDC | 20231005_3eede6d4-a3e1-4dd4-bb18-a721320f7d10.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70771-1415-9 | 70771141509 | 1 BOTTLE, DROPPER in 1 CARTON (70771-1415-9) > 150 mL in 1 BOTTLE, DROPPER | 2018-08-08 | 0000-00-00 | No | No | Current |