Product NDC: | 55289-928 |
Proprietary Name: | PROMETHEGAN |
Non Proprietary Name: | PROMETHAZINE HYDROCHLORIDE |
Active Ingredient(s): | 25 mg/1 & nbsp; PROMETHAZINE HYDROCHLORIDE |
Administration Route(s): | RECTAL |
Dosage Form(s): | SUPPOSITORY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55289-928 |
Labeler Name: | PD-Rx Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040428 |
Marketing Category: | ANDA |
Start Marketing Date: | 20020228 |
Package NDC: | 55289-928-79 |
Package Description: | 1 SUPPOSITORY in 1 BOTTLE, PLASTIC (55289-928-79) |
NDC Code | 55289-928-79 |
Proprietary Name | PROMETHEGAN |
Package Description | 1 SUPPOSITORY in 1 BOTTLE, PLASTIC (55289-928-79) |
Product NDC | 55289-928 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | PROMETHAZINE HYDROCHLORIDE |
Dosage Form Name | SUPPOSITORY |
Route Name | RECTAL |
Start Marketing Date | 20020228 |
Marketing Category Name | ANDA |
Labeler Name | PD-Rx Pharmaceuticals, Inc. |
Substance Name | PROMETHAZINE HYDROCHLORIDE |
Strength Number | 25 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |