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Chlorpromazine Hydrochloride
Chlorpromazine Hydrochloride - 52125-062-02 - (Chlorpromazine Hydrochloride)
Drug Information of Chlorpromazine Hydrochloride
| Product NDC: | 52125-062 |
| Proprietary Name: | Chlorpromazine Hydrochloride |
| Non Proprietary Name: | Chlorpromazine Hydrochloride |
| Active Ingredient(s): | 50 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: | 52125-062 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA083386 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130221 |
Package Information of Chlorpromazine Hydrochloride
| Package NDC: | 52125-062-02 |
| Package Description: | 30 TABLET, SUGAR COATED in 1 BLISTER PACK (52125-062-02) |
NDC Information of Chlorpromazine Hydrochloride
| NDC Code | 52125-062-02 |
| Proprietary Name | Chlorpromazine Hydrochloride |
| Package Description | 30 TABLET, SUGAR COATED in 1 BLISTER PACK (52125-062-02) |
| Product NDC | 52125-062 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Chlorpromazine Hydrochloride |
| Dosage Form Name | TABLET, SUGAR COATED |
| Route Name | ORAL |
| Start Marketing Date | 20130221 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | CHLORPROMAZINE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
