ERGOTAMINE - 0143-2120-05 - (ergotamine tartrate and caffeine)

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Drug Information of ERGOTAMINE

Product NDC: 0143-2120
Proprietary Name: ERGOTAMINE
Non Proprietary Name: ergotamine tartrate and caffeine
Active Ingredient(s): 100; 1    mg/1; mg/1 & nbsp;   ergotamine tartrate and caffeine
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of ERGOTAMINE

Product NDC: 0143-2120
Labeler Name: West-Ward Pharmaceutical Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040510
Marketing Category: ANDA
Start Marketing Date: 20040917

Package Information of ERGOTAMINE

Package NDC: 0143-2120-05
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0143-2120-05)

NDC Information of ERGOTAMINE

NDC Code 0143-2120-05
Proprietary Name ERGOTAMINE
Package Description 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0143-2120-05)
Product NDC 0143-2120
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ergotamine tartrate and caffeine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20040917
Marketing Category Name ANDA
Labeler Name West-Ward Pharmaceutical Corp
Substance Name CAFFEINE; ERGOTAMINE TARTRATE
Strength Number 100; 1
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 ERGOTAMINE


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