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Ipratropium Bromide and Albuterol Sulfate
Ipratropium Bromide and Albuterol Sulfate - 0185-7322-13 - (ipratropium bromide and albuterol sulfate)
Drug Information of Ipratropium Bromide and Albuterol Sulfate
| Product NDC: | 0185-7322 |
| Proprietary Name: | Ipratropium Bromide and Albuterol Sulfate |
| Non Proprietary Name: | ipratropium bromide and albuterol sulfate |
| Active Ingredient(s): | 3; .5 mg/3mL; mg/3mL & nbsp; ipratropium bromide and albuterol sulfate |
| Administration Route(s): | RESPIRATORY (INHALATION) |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ipratropium Bromide and Albuterol Sulfate
| Product NDC: | 0185-7322 |
| Labeler Name: | Eon Labs, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020950 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20010321 |
Package Information of Ipratropium Bromide and Albuterol Sulfate
| Package NDC: | 0185-7322-13 |
| Package Description: | 30 POUCH in 1 CARTON (0185-7322-13) > 1 VIAL in 1 POUCH > 3 mL in 1 VIAL |
NDC Information of Ipratropium Bromide and Albuterol Sulfate
| NDC Code | 0185-7322-13 |
| Proprietary Name | Ipratropium Bromide and Albuterol Sulfate |
| Package Description | 30 POUCH in 1 CARTON (0185-7322-13) > 1 VIAL in 1 POUCH > 3 mL in 1 VIAL |
| Product NDC | 0185-7322 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ipratropium bromide and albuterol sulfate |
| Dosage Form Name | SOLUTION |
| Route Name | RESPIRATORY (INHALATION) |
| Start Marketing Date | 20010321 |
| Marketing Category Name | NDA |
| Labeler Name | Eon Labs, Inc. |
| Substance Name | ALBUTEROL SULFATE; IPRATROPIUM BROMIDE |
| Strength Number | 3; .5 |
| Strength Unit | mg/3mL; mg/3mL |
| Pharmaceutical Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA],Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC] |
