Product NDC: | 54868-5565 |
Proprietary Name: | Atrovent |
Non Proprietary Name: | ipratropium bromide |
Active Ingredient(s): | 21 ug/1 & nbsp; ipratropium bromide |
Administration Route(s): | NASAL |
Dosage Form(s): | SPRAY, METERED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-5565 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020393 |
Marketing Category: | NDA |
Start Marketing Date: | 20060331 |
Package NDC: | 54868-5565-0 |
Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (54868-5565-0) > 345 SPRAY, METERED in 1 BOTTLE, PLASTIC |
NDC Code | 54868-5565-0 |
Proprietary Name | Atrovent |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (54868-5565-0) > 345 SPRAY, METERED in 1 BOTTLE, PLASTIC |
Product NDC | 54868-5565 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | ipratropium bromide |
Dosage Form Name | SPRAY, METERED |
Route Name | NASAL |
Start Marketing Date | 20060331 |
Marketing Category Name | NDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | IPRATROPIUM BROMIDE |
Strength Number | 21 |
Strength Unit | ug/1 |
Pharmaceutical Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA] |