Diclofenac Sodium
- Product NDC
- 76074-501
- 11-digit product format
- 760740501
- Labeler code
- 76074
- Product ID
- 76074-501_b4e24953-24ad-4bbd-8ed0-21484936a843
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac Sodium
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Two Hip Consulting, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2016-03-25
- Marketing end
- 0000-00-00
- Substance
- DICLOFENAC SODIUM
- Active strength
- 3 g/100g
- 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 Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 76074-501-11 | Diclofenac Sodium | 100 g in 1 TUBE | GEL | 100 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76074-501 | DICLOFENAC SODIUM GEL [TWO HIP CONSULTING, LLC] | 4 | Legacy NDC, 1 package rows | 20190207_44b76125-05bd-42fe-a3e8-1d8ec39984e5.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 76074-501-11 | 76074050111 | 100 g in 1 TUBE | 100 g | Historical |