Diclofex DC
- Product NDC
- 51021-379
- 11-digit product format
- 510210379
- Labeler code
- 51021
- Product ID
- 51021-379_0eaadbba-61c8-4880-be7c-fd80849cbf55
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac Sodium and Capsaicin Oleoresin
- Dosage form
- KIT
- Labeler
- Sircle Laboratories, LLC
- Application
- ANDA204132
- Marketing category
- ANDA
- Marketing start
- 2019-01-02
- Marketing end
- 2021-01-31
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 51021-379-01 | ML - Milliliter | 51021-379 | 57e6b439-57ce-41ba-8d9e-17a38579eace | 1 | 2019-04-11 |