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Chlorpromazine Hydrochloride
Chlorpromazine Hydrochloride - 0781-1719-13 - (Chlorpromazine Hydrochloride)
Drug Information of Chlorpromazine Hydrochloride
| Product NDC: | 0781-1719 |
| 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, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Chlorpromazine Hydrochloride
| Product NDC: | 0781-1719 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA080439 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19730103 |
Package Information of Chlorpromazine Hydrochloride
| Package NDC: | 0781-1719-13 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (0781-1719-13) > 10 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of Chlorpromazine Hydrochloride
| NDC Code | 0781-1719-13 |
| Proprietary Name | Chlorpromazine Hydrochloride |
| Package Description | 10 BLISTER PACK in 1 CARTON (0781-1719-13) > 10 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 0781-1719 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Chlorpromazine Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19730103 |
| 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] |
