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Chlordiazepoxide Hydrochloride and Clidinium Bromide - 68682-409-10 - (Chlordiazepoxide Hydrochloride and Clidinium Bromide)

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Drug Information of Chlordiazepoxide Hydrochloride and Clidinium Bromide

Product NDC: 68682-409
Proprietary Name: Chlordiazepoxide Hydrochloride and 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 and Clidinium Bromide

Product NDC: 68682-409
Labeler Name: Oceanside Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA012750
Marketing Category: NDA
Start Marketing Date: 20090923

Package Information of Chlordiazepoxide Hydrochloride and Clidinium Bromide

Package NDC: 68682-409-10
Package Description: 100 CAPSULE in 1 BOTTLE, PLASTIC (68682-409-10)

NDC Information of Chlordiazepoxide Hydrochloride and Clidinium Bromide

NDC Code 68682-409-10
Proprietary Name Chlordiazepoxide Hydrochloride and Clidinium Bromide
Package Description 100 CAPSULE in 1 BOTTLE, PLASTIC (68682-409-10)
Product NDC 68682-409
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Chlordiazepoxide Hydrochloride and Clidinium Bromide
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20090923
Marketing Category Name NDA
Labeler Name Oceanside 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],Anticholinergic [EPC],Decreased Parasympathetic Acetylcholine Activity [PE],GI Motility Alteration [PE],Digestive/GI System Activity Alteration [PE],Cholinergic Antagonists [MoA]

Complete Information of Chlordiazepoxide Hydrochloride and Clidinium Bromide


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