Lidocaine 51672-3008-05

Package NDC

51672-3008-05

Manufacturer: Sun Pharmaceutical Industries, Inc.
Dosage Form: Ointment
Route: Topical
Product Type: Human Prescription Drug
Marketing Start: August 17, 1981
Listing Expires: December 31, 2027
Application: ANDA086724

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Active Ingredients

Ingredient	Strength
Lidocaine	50 mg/g

Drug Class

Amide Local Anesthetic [EPC]Antiarrhythmic [EPC]Amide Local Anesthetic [EPC]

Selected Package

51672-3008-05Selected

1 JAR in 1 CARTON (51672-3008-5) / 50 g in 1 JAR