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Chlordiazepoxide Hydrochloride/Clidinium Bromide - 76439-302-10 - (Chlordiazepoxide Hydrochloride and Clidinium Bromide)

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Drug Information of Chlordiazepoxide Hydrochloride/Clidinium Bromide

Product NDC: 76439-302
Proprietary Name: Chlordiazepoxide Hydrochloride/Clidinium Bromide
Non Proprietary Name: Chlordiazepoxide Hydrochloride and Clidinium Bromide
Active Ingredient(s): 5; 2.5    mg/1; mg/1 & nbsp;   Chlordiazepoxide Hydrochloride and Clidinium Bromide
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Chlordiazepoxide Hydrochloride/Clidinium Bromide

Product NDC: 76439-302
Labeler Name: Virtus Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20120608

Package Information of Chlordiazepoxide Hydrochloride/Clidinium Bromide

Package NDC: 76439-302-10
Package Description: 100 CAPSULE in 1 BOTTLE (76439-302-10)

NDC Information of Chlordiazepoxide Hydrochloride/Clidinium Bromide

NDC Code 76439-302-10
Proprietary Name Chlordiazepoxide Hydrochloride/Clidinium Bromide
Package Description 100 CAPSULE in 1 BOTTLE (76439-302-10)
Product NDC 76439-302
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Chlordiazepoxide Hydrochloride and Clidinium Bromide
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120608
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Virtus Pharmaceuticals
Substance Name CHLORDIAZEPOXIDE HYDROCHLORIDE; CLIDINIUM BROMIDE
Strength Number 5; 2.5
Strength Unit mg/1; mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Chlordiazepoxide Hydrochloride/Clidinium Bromide


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