50090-6186 NDC - LIDOCAINE VISCOUS (LIDOCAINE HYDROCHLORIDE)

Drug Information

Product NDC: 50090-6186
Proprietary Name: Lidocaine Viscous
Non Proprietary Name: Lidocaine Hydrochloride
Active Ingredient(s): 20 mg/mL LIDOCAINE HYDROCHLORIDE
Administration Route(s): ORAL; TOPICAL
Dosage Form(s): SOLUTION
Pharmacy Class(es): Amide Local Anesthetic [EPC]; Amides [CS]; Antiarrhythmic [EPC]; Local Anesthesia [PE]

Labeler Information

Field Name	Field Value
Labeler Name:	A-S Medication Solutions
Product Type:	HUMAN PRESCRIPTION DRUG
FDA Application Number:	ANDA088802
Marketing Category:	ANDA
Start Marketing Date:	4/26/1985

Package Information

No.	Package Code	Package Description	Billing Unit
1	50090-6186-0	1 BOTTLE in 1 CARTON (50090-6186-0) / 100 mL in 1 BOTTLE	ML

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	50090-6186	The translation of the dosage form Code submitted by the firm.
PRODUCT TYPE NAME	HUMAN PRESCRIPTION DRUG	This is the date that the labeler indicates was the start of its marketing of the drug product.
PROPRIETARY NAME	Lidocaine Viscous	Name of Company corresponding to the labeler code segment of the Product NDC.
NON PROPRIETARY NAME	Lidocaine Hydrochloride	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	SOLUTION	The translation of the dosage form Code submitted by the firm.
ROUTE NAME	ORAL; TOPICAL	The translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE	4/26/1985	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	ANDA	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
APPLICATION NUMBER	ANDA088802	This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAME	A-S Medication Solutions	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	LIDOCAINE HYDROCHLORIDE	An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH	20
ACTIVE INGRED UNIT	mg/mL
PHARM CLASSES	Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]

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This page was last updated on: 11/21/2025

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