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