Product NDC: | 0378-6989 |
Proprietary Name: | Ipratropium Bromide |
Non Proprietary Name: | ipratropium bromide |
Active Ingredient(s): | 500 ug/2.5mL & nbsp; ipratropium bromide |
Administration Route(s): | RESPIRATORY (INHALATION) |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0378-6989 |
Labeler Name: | Mylan Pharmaceuticals Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075693 |
Marketing Category: | ANDA |
Start Marketing Date: | 20101109 |
Package NDC: | 0378-6989-62 |
Package Description: | 25 POUCH in 1 CARTON (0378-6989-62) > 1 VIAL in 1 POUCH > 2.5 mL in 1 VIAL |
NDC Code | 0378-6989-62 |
Proprietary Name | Ipratropium Bromide |
Package Description | 25 POUCH in 1 CARTON (0378-6989-62) > 1 VIAL in 1 POUCH > 2.5 mL in 1 VIAL |
Product NDC | 0378-6989 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | ipratropium bromide |
Dosage Form Name | SOLUTION |
Route Name | RESPIRATORY (INHALATION) |
Start Marketing Date | 20101109 |
Marketing Category Name | ANDA |
Labeler Name | Mylan Pharmaceuticals Inc. |
Substance Name | IPRATROPIUM BROMIDE |
Strength Number | 500 |
Strength Unit | ug/2.5mL |
Pharmaceutical Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA] |