Diclofenac sodium
- Product NDC
- 63187-762
- 11-digit product format
- 631870762
- Labeler code
- 63187
- Product ID
- 63187-762_490d4045-f6a8-4c92-8b02-28d9942ddec0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Proficient Rx LP
- Application
- ANDA208077
- Marketing category
- ANDA
- Marketing start
- 2016-03-21
- Marketing end
- 0000-00-00
- Substance
- DICLOFENAC SODIUM
- Active strength
- 10 mg/g
- 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
- 2020-12-31
- 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 |
|---|
| 63187-762 | DICLOFENAC SODIUM (DICLOFENAC) GEL [PROFICIENT RX LP] | 2 | Legacy NDC | 20191115_968f4686-23b4-4b4a-9fe5-2eee7a370010.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63187-762-00 | 63187076200 | 1 TUBE in 1 CARTON (63187-762-00) > 100 g in 1 TUBE | 1 tube | 2016-10-03 | 0000-00-00 | No | No | Current |