Lidozion
- Product NDC
- 51021-164
- 11-digit product format
- 510210164
- Labeler code
- 51021
- Product ID
- 51021-164_9273e71f-f418-2ff6-e053-2a95a90a9324
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lidocaine HCL External Lotion
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Sircle Laboratories, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2018-04-02
- Marketing end
- 2020-06-01
- Substance
- LIDOCAINE HYDROCHLORIDE
- Active strength
- 30 mg/177mL
- Pharmacologic classes
- Amide Local Anesthetic [EPC],Amides [CS],Antiarrhythmic [EPC],Local Anesthesia [PE]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record