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chlorpromazine hydrochloride
chlorpromazine hydrochloride - 67046-104-30 - (chlorpromazine hydrochloride)
Drug Information of chlorpromazine hydrochloride
| Product NDC: | 67046-104 |
| 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) |
Labeler Information of chlorpromazine hydrochloride
| Product NDC: | 67046-104 |
| Labeler Name: | Contract Pharmacy Services-PA |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA084114 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100225 |
Package Information of chlorpromazine hydrochloride
| Package NDC: | 67046-104-30 |
| Package Description: | 30 TABLET, SUGAR COATED in 1 BLISTER PACK (67046-104-30) |
NDC Information of chlorpromazine hydrochloride
| NDC Code | 67046-104-30 |
| Proprietary Name | chlorpromazine hydrochloride |
| Package Description | 30 TABLET, SUGAR COATED in 1 BLISTER PACK (67046-104-30) |
| Product NDC | 67046-104 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | chlorpromazine hydrochloride |
| Dosage Form Name | TABLET, SUGAR COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100225 |
| Marketing Category Name | ANDA |
| Labeler Name | Contract Pharmacy Services-PA |
| Substance Name | CHLORPROMAZINE HYDROCHLORIDE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
