Ergoloid Mesylates Tablets USP oral 1mg

Ergoloid Mesylates by

Drug Labeling and Warnings

Ergoloid Mesylates by is a Prescription medication manufactured, distributed, or labeled by Frontida BioPharm, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ERGOLOID MESYLATES- dihydroergocornine mesylate, dihydroergocristine mesylate, dihydro-.alpha.-ergocryptine mesylate, and dihydro-.beta.-ergocryptine mesylate tablet 
Frontida BioPharm, Inc.

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Ergoloid Mesylates Tablets USP oral 1mg

Principal Display Panel

NDC: 71557-037-10
Ergoloid Mesylates Tablets USP
(oral)
1mg
Rx Only
100 Tablets
SUN PHARMA

ERGOLOID MESYLATES 
dihydroergocornine mesylate, dihydroergocristine mesylate, dihydro-.alpha.-ergocryptine mesylate, and dihydro-.beta.-ergocryptine mesylate tablet

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 71557-037
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Dihydroergocornine Mesylate (UNII: 42RX8KPW29) (Dihydroergocornine - UNII:IK4C1OC8NE)	Dihydroergocornine Mesylate	0.333 mg
Dihydroergocristine Mesylate (UNII: DS7CL18UAM) (Dihydroergocristine - UNII:05D48LUM4Z)	Dihydroergocristine Mesylate	0.333 mg
Dihydro-.alpha.-ergocryptine mesylate (UNII: Z4I7BU58DN) (Dihydro-.alpha.-ergocryptine - UNII:202229IR8Y)	Dihydro-.alpha.-ergocryptine mesylate	0.222 mg
Dihydro-.beta.-ergocryptine mesylate (UNII: 79Y4U49I29) (Epicriptine - UNII:5M64643B5U)	Dihydro-.beta.-ergocryptine mesylate	0.111 mg

Inactive Ingredients
Ingredient Name	Strength
BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)
STARCH, CORN (UNII: O8232NY3SJ)
HYDROGENATED COTTONSEED OIL (UNII: Z82Y2C65EA)
LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)
MANNITOL (UNII: 3OWL53L36A)
POVIDONE K90 (UNII: RDH86HJV5Z)
STEARIC ACID (UNII: 4ELV7Z65AP)
TALC (UNII: 7SEV7J4R1U)

Product Characteristics
Color	WHITE	Score	no score
Shape	ROUND	Size	8mm
Flavor		Imprint Code	MP;20
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71557-037-10	100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA081113	06/01/2017

Labeler - Frontida BioPharm, Inc. (080243260)

Revised: 7/2019

Document Id: 3208d4dc-d9dd-4ca9-87dd-1b8611873658

34391-3

Set id: af8732ad-6260-42c7-823f-2c74bf34c021

Version: 1

Effective Time: 20190730

 

Frontida BioPharm, Inc.