Product NDC: | 54868-5751 |
Proprietary Name: | Ipratropium Bromide |
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: | 54868-5751 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076025 |
Marketing Category: | ANDA |
Start Marketing Date: | 20070124 |
Package NDC: | 54868-5751-0 |
Package Description: | 1 BOTTLE, SPRAY in 1 CARTON (54868-5751-0) > 345 SPRAY, METERED in 1 BOTTLE, SPRAY |
NDC Code | 54868-5751-0 |
Proprietary Name | Ipratropium Bromide |
Package Description | 1 BOTTLE, SPRAY in 1 CARTON (54868-5751-0) > 345 SPRAY, METERED in 1 BOTTLE, SPRAY |
Product NDC | 54868-5751 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Ipratropium Bromide |
Dosage Form Name | SPRAY, METERED |
Route Name | NASAL |
Start Marketing Date | 20070124 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | IPRATROPIUM BROMIDE |
Strength Number | 21 |
Strength Unit | ug/1 |
Pharmaceutical Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA] |