Product NDC: | 0832-0303 |
Proprietary Name: | Chlorpromazine Hydrochloride |
Non Proprietary Name: | Chlorpromazine Hydrochloride |
Active Ingredient(s): | 100 mg/1 & nbsp; Chlorpromazine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, SUGAR COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0832-0303 |
Labeler Name: | Upsher-Smith Laboratories, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA084114 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110803 |
Package NDC: | 0832-0303-10 |
Package Description: | 1000 TABLET, SUGAR COATED in 1 BOTTLE (0832-0303-10) |
NDC Code | 0832-0303-10 |
Proprietary Name | Chlorpromazine Hydrochloride |
Package Description | 1000 TABLET, SUGAR COATED in 1 BOTTLE (0832-0303-10) |
Product NDC | 0832-0303 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Chlorpromazine Hydrochloride |
Dosage Form Name | TABLET, SUGAR COATED |
Route Name | ORAL |
Start Marketing Date | 20110803 |
Marketing Category Name | ANDA |
Labeler Name | Upsher-Smith Laboratories, Inc. |
Substance Name | CHLORPROMAZINE HYDROCHLORIDE |
Strength Number | 100 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |