Product NDC: | 35356-325 |
Proprietary Name: | Prochlorperazine Maleate |
Non Proprietary Name: | Prochlorperazine Maleate |
Active Ingredient(s): | 10 mg/1 & nbsp; Prochlorperazine Maleate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 35356-325 |
Labeler Name: | Lake Erie Medical & Surgical Supply DBA Quality Care Prodcuts LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040120 |
Marketing Category: | ANDA |
Start Marketing Date: | 20111206 |
Package NDC: | 35356-325-05 |
Package Description: | 5 TABLET, FILM COATED in 1 BOTTLE (35356-325-05) |
NDC Code | 35356-325-05 |
Proprietary Name | Prochlorperazine Maleate |
Package Description | 5 TABLET, FILM COATED in 1 BOTTLE (35356-325-05) |
Product NDC | 35356-325 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Prochlorperazine Maleate |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20111206 |
Marketing Category Name | ANDA |
Labeler Name | Lake Erie Medical & Surgical Supply DBA Quality Care Prodcuts LLC |
Substance Name | PROCHLORPERAZINE MALEATE |
Strength Number | 10 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |