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Chlordiazepoxide and Amitriptyline Hydrochloride
Chlordiazepoxide and Amitriptyline Hydrochloride - 0378-0211-05 - (chlordiazepoxide and amitriptyline hydrochloride)
Drug Information of Chlordiazepoxide and Amitriptyline Hydrochloride
| Product NDC: | 0378-0211 |
| Proprietary Name: | Chlordiazepoxide and Amitriptyline Hydrochloride |
| Non Proprietary Name: | chlordiazepoxide and amitriptyline hydrochloride |
| Active Ingredient(s): | 12.5; 5 mg/1; mg/1 & nbsp; chlordiazepoxide and amitriptyline hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Chlordiazepoxide and Amitriptyline Hydrochloride
| Product NDC: | 0378-0211 |
| Labeler Name: | Mylan Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA071297 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100127 |
Package Information of Chlordiazepoxide and Amitriptyline Hydrochloride
| Package NDC: | 0378-0211-05 |
| Package Description: | 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0211-05) |
NDC Information of Chlordiazepoxide and Amitriptyline Hydrochloride
| NDC Code | 0378-0211-05 |
| Proprietary Name | Chlordiazepoxide and Amitriptyline Hydrochloride |
| Package Description | 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0211-05) |
| Product NDC | 0378-0211 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | chlordiazepoxide and amitriptyline hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100127 |
| Marketing Category Name | ANDA |
| Labeler Name | Mylan Pharmaceuticals Inc. |
| Substance Name | AMITRIPTYLINE HYDROCHLORIDE; CHLORDIAZEPOXIDE |
| Strength Number | 12.5; 5 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient],Tricyclic Antidepressant [EPC] |
