diclofenac sodium
- Product NDC
- 72162-1391
- 11-digit product format
- 721621391
- Labeler code
- 72162
- Product ID
- 72162-1391_333b3bf8-b59e-4019-8bf9-8a781bce3c56
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- diclofenac sodium
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA210893
- Marketing category
- ANDA
- Marketing start
- 2018-11-27
- Substance
- DICLOFENAC SODIUM
- Active strength
- 30 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
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- diclofenac sodium
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DICLOFENAC SODIUM | 30 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | QTG126297Q |
| Rxcui | 855642 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-1391-1 | diclofenac sodium | 1 in 1 CARTON | GEL | 1 | | 102 |
| 72162-1391-1 | diclofenac sodium | 100 g in 1 TUBE | GEL | 100 | | 102 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-1391 | DICLOFENAC SODIUM GEL [BRYANT RANCH PREPACK] | 102 | Current NDC, 2 package rows | 20241108_bf372e32-0902-447f-9673-00a3fcf0064c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1391-1 | 72162139101 | 1 TUBE in 1 CARTON (72162-1391-1) / 100 g in 1 TUBE | 1 tube | 2018-11-27 | No | No | Historical |