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Chlorpromazine hydrochloride
Chlorpromazine hydrochloride - 0641-1398-35 - (Chlorpromazine hydrochloride)
Drug Information of Chlorpromazine hydrochloride
| Product NDC: | 0641-1398 |
| Proprietary Name: | Chlorpromazine hydrochloride |
| Non Proprietary Name: | Chlorpromazine hydrochloride |
| Active Ingredient(s): | 25 mg/mL & nbsp; Chlorpromazine hydrochloride |
| Administration Route(s): | INTRAMUSCULAR |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Chlorpromazine hydrochloride
| Product NDC: | 0641-1398 |
| Labeler Name: | West-ward Pharmaceutical Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA083329 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19740725 |
Package Information of Chlorpromazine hydrochloride
| Package NDC: | 0641-1398-35 |
| Package Description: | 25 AMPULE in 1 CARTON (0641-1398-35) > 2 mL in 1 AMPULE (0641-1398-31) |
NDC Information of Chlorpromazine hydrochloride
| NDC Code | 0641-1398-35 |
| Proprietary Name | Chlorpromazine hydrochloride |
| Package Description | 25 AMPULE in 1 CARTON (0641-1398-35) > 2 mL in 1 AMPULE (0641-1398-31) |
| Product NDC | 0641-1398 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Chlorpromazine hydrochloride |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR |
| Start Marketing Date | 19740725 |
| Marketing Category Name | ANDA |
| Labeler Name | West-ward Pharmaceutical Corp. |
| Substance Name | CHLORPROMAZINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
