Diclofenac Sodium
- Product NDC
- 58602-601
- 11-digit product format
- 586020601
- Labeler code
- 58602
- Product ID
- 58602-601_3aa8483e-7655-4a3f-8b95-f4520b9567b1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Diclofenac
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Aurohealth LLC
- Application
- ANDA204306
- Marketing category
- ANDA
- Marketing start
- 2020-08-06
- Marketing end
- 0000-00-00
- Substance
- DICLOFENAC SODIUM
- Active strength
- 10 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 58602-601-07 | 58602060107 | 1 TUBE in 1 CARTON (58602-601-07) > 100 g in 1 TUBE | 1 tube | 2020-08-06 | 0000-00-00 | No | No | Current |