Lexixryl
- Product NDC
- 69621-365
- 11-digit product format
- 696210365
- Labeler code
- 69621
- Product ID
- 69621-365_054ab420-32ab-4237-b640-abada8896e9c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac Sodium
- Dosage form
- KIT
- Labeler
- Shoreline Pharmaceuticals, Inc.
- Application
- ANDA202769
- Marketing category
- ANDA
- Marketing start
- 2016-11-08
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 69621-365-00 | EA - Each | 69621-365 | 2d40c36a-eafb-44ac-aadd-20ca8a12f7d4 | 1 | 2017-05-04 |