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Chlordiazepoxide and Amitriptyline HCl
Chlordiazepoxide and Amitriptyline HCl - 49884-265-01 - (Chlordiazepoxide and Amitriptyline hydrochloride)
Drug Information of Chlordiazepoxide and Amitriptyline HCl
| Product NDC: | 49884-265 |
| Proprietary Name: | Chlordiazepoxide and Amitriptyline HCl |
| 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 |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Chlordiazepoxide and Amitriptyline HCl
| Product NDC: | 49884-265 |
| Labeler Name: | Par Pharmaceutical Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA072277 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19880509 |
Package Information of Chlordiazepoxide and Amitriptyline HCl
| Package NDC: | 49884-265-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (49884-265-01) |
NDC Information of Chlordiazepoxide and Amitriptyline HCl
| NDC Code | 49884-265-01 |
| Proprietary Name | Chlordiazepoxide and Amitriptyline HCl |
| Package Description | 100 TABLET in 1 BOTTLE (49884-265-01) |
| Product NDC | 49884-265 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Chlordiazepoxide and Amitriptyline hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19880509 |
| Marketing Category Name | ANDA |
| Labeler Name | Par Pharmaceutical 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] |
