Lidocaine Hydrochloride
- Product NDC
- 58980-822
- 11-digit product format
- 589800822
- Labeler code
- 58980
- Product ID
- 58980-822_adb7a8f8-57b9-426c-a1e5-6d0285d85f10
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lidocaine Hydrochloride
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Stratus Pharamceuticals
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2012-03-01
- Marketing end
- 0000-00-00
- Substance
- LIDOCAINE HYDROCHLORIDE
- Active strength
- 5 mL/177mL
- Pharmacologic classes
- Amide Local Anesthetic [EPC],Amides [CS],Antiarrhythmic [EPC],Local Anesthesia [PE]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#