Home
>
National Drug Code (NDC)
>
Chlorpromazine Hydrochloride
Chlorpromazine Hydrochloride - 0781-5917-01 - (Chlorpromazine Hydrochloride)
Drug Information of Chlorpromazine Hydrochloride
| Product NDC: | 0781-5917 |
| Proprietary Name: | Chlorpromazine Hydrochloride |
| Non Proprietary Name: | Chlorpromazine Hydrochloride |
| Active Ingredient(s): | 200 mg/1 & nbsp; Chlorpromazine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, SUGAR COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Chlorpromazine Hydrochloride
| Product NDC: | 0781-5917 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA084115 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19740709 |
Package Information of Chlorpromazine Hydrochloride
| Package NDC: | 0781-5917-01 |
| Package Description: | 100 TABLET, SUGAR COATED in 1 BOTTLE (0781-5917-01) |
NDC Information of Chlorpromazine Hydrochloride
| NDC Code | 0781-5917-01 |
| Proprietary Name | Chlorpromazine Hydrochloride |
| Package Description | 100 TABLET, SUGAR COATED in 1 BOTTLE (0781-5917-01) |
| Product NDC | 0781-5917 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Chlorpromazine Hydrochloride |
| Dosage Form Name | TABLET, SUGAR COATED |
| Route Name | ORAL |
| Start Marketing Date | 19740709 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | CHLORPROMAZINE HYDROCHLORIDE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
