Product NDC: | 54868-4721 |
Proprietary Name: | Prochlorperazine Maleate |
Non Proprietary Name: | Prochlorperazine Maleate |
Active Ingredient(s): | 5 mg/1 & nbsp; Prochlorperazine Maleate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-4721 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040101 |
Marketing Category: | ANDA |
Start Marketing Date: | 20030210 |
Package NDC: | 54868-4721-4 |
Package Description: | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-4721-4) |
NDC Code | 54868-4721-4 |
Proprietary Name | Prochlorperazine Maleate |
Package Description | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-4721-4) |
Product NDC | 54868-4721 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Prochlorperazine Maleate |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20030210 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | PROCHLORPERAZINE MALEATE |
Strength Number | 5 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |