Lidocaine Hydrochloride
- Product NDC
- 63739-694
- 11-digit product format
- 637390694
- Labeler code
- 63739
- Product ID
- 63739-694_acf79600-f78d-469e-a8a4-0ae3616ed2d9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lidocaine Hydrochloride
- Dosage form
- SOLUTION
- Route
- OROPHARYNGEAL
- Labeler
- McKesson Corporation dba SKY Packaging
- Application
- ANDA040708
- Marketing category
- ANDA
- Marketing start
- 2007-02-27
- Marketing end
- 0000-00-00
- Substance
- LIDOCAINE HYDROCHLORIDE ANHYDROUS
- Active strength
- 20 mg/mL
- 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
FDA-Initiated Inactive NDC Indexing#