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PROCHLORPERAZINE
PROCHLORPERAZINE - 16590-327-30 - (PROCHLORPERAZINE MALEATE)
Drug Information of PROCHLORPERAZINE
| Product NDC: | 16590-327 |
| Proprietary Name: | PROCHLORPERAZINE |
| Non Proprietary Name: | PROCHLORPERAZINE MALEATE |
| Active Ingredient(s): | 10 mg/1 & nbsp; PROCHLORPERAZINE MALEATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PROCHLORPERAZINE
| Product NDC: | 16590-327 |
| Labeler Name: | STAT RX USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040120 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090729 |
Package Information of PROCHLORPERAZINE
| Package NDC: | 16590-327-30 |
| Package Description: | 30 TABLET in 1 BOTTLE, PLASTIC (16590-327-30) |
NDC Information of PROCHLORPERAZINE
| NDC Code | 16590-327-30 |
| Proprietary Name | PROCHLORPERAZINE |
| Package Description | 30 TABLET in 1 BOTTLE, PLASTIC (16590-327-30) |
| Product NDC | 16590-327 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PROCHLORPERAZINE MALEATE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090729 |
| Marketing Category Name | ANDA |
| Labeler Name | STAT RX USA LLC |
| Substance Name | PROCHLORPERAZINE MALEATE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
