MIGERGOT - 0713-0166-12 - (Ergotamine Tartrate and Caffeine)

Alphabetical Index


Drug Information of MIGERGOT

Product NDC: 0713-0166
Proprietary Name: MIGERGOT
Non Proprietary Name: Ergotamine Tartrate and Caffeine
Active Ingredient(s): 100; 2    mg/1; mg/1 & nbsp;   Ergotamine Tartrate and Caffeine
Administration Route(s): RECTAL
Dosage Form(s): SUPPOSITORY
Coding System: National Drug Codes(NDC)

Labeler Information of MIGERGOT

Product NDC: 0713-0166
Labeler Name: G & W LABORATORIES, INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA086557
Marketing Category: ANDA
Start Marketing Date: 19831030

Package Information of MIGERGOT

Package NDC: 0713-0166-12
Package Description: 12 SUPPOSITORY in 1 BOX (0713-0166-12)

NDC Information of MIGERGOT

NDC Code 0713-0166-12
Proprietary Name MIGERGOT
Package Description 12 SUPPOSITORY in 1 BOX (0713-0166-12)
Product NDC 0713-0166
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ergotamine Tartrate and Caffeine
Dosage Form Name SUPPOSITORY
Route Name RECTAL
Start Marketing Date 19831030
Marketing Category Name ANDA
Labeler Name G & W LABORATORIES, INC.
Substance Name CAFFEINE; ERGOTAMINE TARTRATE
Strength Number 100; 2
Strength Unit mg/1; mg/1
Pharmaceutical Classes Ergotamine Derivative [EPC],Ergotamines [Chemical/Ingredient],Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE],Methylxanthine [EPC],Xanthines [Chemical/Ingredient]

Complete Information of MIGERGOT


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