| NDC Code: |
49884-265 |
| Proprietary Name: |
Chlordiazepoxide and Amitriptyline HCl |
| Suffix: |
|
| Non-Proprietary Name: |
Chlordiazepoxide and Amitriptyline hydrochloride |
| Dosage Form: |
TABLET |
| Method: |
ORAL |
| Original Marketing Date: |
09-05-1988 |
| Category Name: |
ANDA |
| Application Number: |
ANDA072277 |
| Labeler: |
PAR PHARMACEUTICAL INC |
| Substance Name: |
AMITRIPTYLINE HYDROCHLORIDE; CHLORDIAZEPOXIDE |
| Active Numerator Strength: |
12.5; 5 |
| Active Ingredient Unit: |
mg/1; mg/1 |
| Pharm Classes: |
Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient],Tricyclic Antidepressant [EPC] |
| DEA Schedule: |
CIV |
