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CHLORPROMAZINE HYDROCHLORIDE
CHLORPROMAZINE HYDROCHLORIDE - 24236-323-20 - (CHLORPROMAZINE HYDROCHLORIDE)
Drug Information of CHLORPROMAZINE HYDROCHLORIDE
| Product NDC: | 24236-323 |
| Proprietary Name: | CHLORPROMAZINE HYDROCHLORIDE |
| Non Proprietary Name: | CHLORPROMAZINE HYDROCHLORIDE |
| Active Ingredient(s): | 25 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: | 24236-323 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA084112 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101216 |
Package Information of CHLORPROMAZINE HYDROCHLORIDE
| Package NDC: | 24236-323-20 |
| Package Description: | 100 TABLET, SUGAR COATED in 1 CANISTER (24236-323-20) |
NDC Information of CHLORPROMAZINE HYDROCHLORIDE
| NDC Code | 24236-323-20 |
| Proprietary Name | CHLORPROMAZINE HYDROCHLORIDE |
| Package Description | 100 TABLET, SUGAR COATED in 1 CANISTER (24236-323-20) |
| Product NDC | 24236-323 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CHLORPROMAZINE HYDROCHLORIDE |
| Dosage Form Name | TABLET, SUGAR COATED |
| Route Name | ORAL |
| Start Marketing Date | 20101216 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | CHLORPROMAZINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
