Professional Medicated DNA Collection
- Product NDC
- 51021-440
- 11-digit product format
- 510210440
- Labeler code
- 51021
- Product ID
- 51021-440_baa2b544-9a16-45be-8eab-3535fced5545
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lidocaine Hydrochloride and Glycerin
- Dosage form
- KIT
- Labeler
- Sircle Laboratories, LLC
- Application
- ANDA040014
- Marketing category
- ANDA
- Marketing start
- 1995-07-10
- 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