Product NDC: | 68258-3011 |
Proprietary Name: | Promethazine Hydrochloride |
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: | 68258-3011 |
Labeler Name: | Dispensing Solutions Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA123456 |
Marketing Category: | ANDA |
Start Marketing Date: | 20031219 |
Package NDC: | 68258-3011-4 |
Package Description: | 1 BLISTER PACK in 1 CARTON (68258-3011-4) > 4 SUPPOSITORY in 1 BLISTER PACK |
NDC Code | 68258-3011-4 |
Proprietary Name | Promethazine Hydrochloride |
Package Description | 1 BLISTER PACK in 1 CARTON (68258-3011-4) > 4 SUPPOSITORY in 1 BLISTER PACK |
Product NDC | 68258-3011 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | PROMETHAZINE HYDROCHLORIDE |
Dosage Form Name | SUPPOSITORY |
Route Name | RECTAL |
Start Marketing Date | 20031219 |
Marketing Category Name | ANDA |
Labeler Name | Dispensing Solutions Inc. |
Substance Name | PROMETHAZINE HYDROCHLORIDE |
Strength Number | 25 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |