Orbivan - 0095-7029-09 - (Acetaminophen, butalbital and caffeine)

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Drug Information of Orbivan

Product NDC: 0095-7029
Proprietary Name: Orbivan
Non Proprietary Name: Acetaminophen, butalbital and caffeine
Active Ingredient(s): 300; 50; 40    mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, butalbital and caffeine
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Orbivan

Product NDC: 0095-7029
Labeler Name: ECR Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040885
Marketing Category: ANDA
Start Marketing Date: 20120821

Package Information of Orbivan

Package NDC: 0095-7029-09
Package Description: 1 CAPSULE in 1 POUCH (0095-7029-09)

NDC Information of Orbivan

NDC Code 0095-7029-09
Proprietary Name Orbivan
Package Description 1 CAPSULE in 1 POUCH (0095-7029-09)
Product NDC 0095-7029
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Acetaminophen, butalbital and caffeine
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120821
Marketing Category Name ANDA
Labeler Name ECR Pharmaceuticals
Substance Name ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Strength Number 300; 50; 40
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes Barbiturate [EPC],Barbiturates [Chemical/Ingredient],Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE],Methylxanthine [EPC],Xanthines [Chemical/Ingredient]

Complete Information of Orbivan


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