DICLOFENAC SODIUM
- Product NDC
- 71205-618
- 11-digit product format
- 712050618
- Labeler code
- 71205
- Product ID
- 71205-618_0abc944e-a435-4f77-922d-380e5aab6c5f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- diclofenac sodium
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Proficient Rx LP
- Application
- ANDA211253
- Marketing category
- ANDA
- Marketing start
- 2019-05-20
- Marketing end
- 0000-00-00
- Substance
- DICLOFENAC SODIUM
- Active strength
- 10 mg/g
- 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 |
|---|
| 71205-618 | DICLOFENAC SODIUM GEL [PROFICIENT RX LP] | 2 | Legacy NDC | 20220525_94880e4f-6b55-493c-b8b7-9d74df1c4896.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-618-00 | 71205061800 | 1 TUBE in 1 CARTON (71205-618-00) > 100 g in 1 TUBE | 1 tube | 2021-11-04 | 0000-00-00 | No | No | Current |