Product NDC: | 52389-136 |
Proprietary Name: | Diurex |
Non Proprietary Name: | Pamabrom |
Active Ingredient(s): | 50 mg/1 & nbsp; Pamabrom |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, LIQUID FILLED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52389-136 |
Labeler Name: | Alva-Amco Pharmacal Companies, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part357 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20000410 |
Package NDC: | 52389-136-24 |
Package Description: | 1 BLISTER PACK in 1 CARTON (52389-136-24) > 24 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (52389-136-02) |
NDC Code | 52389-136-24 |
Proprietary Name | Diurex |
Package Description | 1 BLISTER PACK in 1 CARTON (52389-136-24) > 24 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (52389-136-02) |
Product NDC | 52389-136 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Pamabrom |
Dosage Form Name | CAPSULE, LIQUID FILLED |
Route Name | ORAL |
Start Marketing Date | 20000410 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Alva-Amco Pharmacal Companies, Inc. |
Substance Name | PAMABROM |
Strength Number | 50 |
Strength Unit | mg/1 |
Pharmaceutical Classes |