Lidocaine
- Product NDC
- 71335-0994
- 11-digit product format
- 713350994
- Labeler code
- 71335
- Product ID
- 71335-0994_d62ee74f-a1b2-4fff-bb3c-3a2885363a0a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lidocaine
- Dosage form
- PATCH
- Route
- CUTANEOUS
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA200675
- Marketing category
- ANDA
- Marketing start
- 2016-02-29
- Marketing end
- 0000-00-00
- Substance
- LIDOCAINE
- Active strength
- 50 mg/g
- Pharmacologic classes
- Amide Local Anesthetic [EPC],Amides [CS],Antiarrhythmic [EPC],Local Anesthesia [PE]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record