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Ipratropium Bromide
Ipratropium Bromide - 76204-100-30 - (Ipratropium Bromide)
Drug Information of Ipratropium Bromide
| Product NDC: | 76204-100 |
| Proprietary Name: | Ipratropium Bromide |
| Non Proprietary Name: | Ipratropium Bromide |
| Active Ingredient(s): | .5 mg/2.5mL & nbsp; Ipratropium Bromide |
| Administration Route(s): | RESPIRATORY (INHALATION) |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ipratropium Bromide
| Product NDC: | 76204-100 |
| Labeler Name: | Ritedose Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075693 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110201 |
Package Information of Ipratropium Bromide
| Package NDC: | 76204-100-30 |
| Package Description: | 1 POUCH in 1 CARTON (76204-100-30) > 30 AMPULE in 1 POUCH > 2.5 mL in 1 AMPULE |
NDC Information of Ipratropium Bromide
| NDC Code | 76204-100-30 |
| Proprietary Name | Ipratropium Bromide |
| Package Description | 1 POUCH in 1 CARTON (76204-100-30) > 30 AMPULE in 1 POUCH > 2.5 mL in 1 AMPULE |
| Product NDC | 76204-100 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ipratropium Bromide |
| Dosage Form Name | SOLUTION |
| Route Name | RESPIRATORY (INHALATION) |
| Start Marketing Date | 20110201 |
| Marketing Category Name | ANDA |
| Labeler Name | Ritedose Pharmaceuticals, LLC |
| Substance Name | IPRATROPIUM BROMIDE |
| Strength Number | .5 |
| Strength Unit | mg/2.5mL |
| Pharmaceutical Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA] |
