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Ipratropium Bromide and Albuterol Sulfate
Ipratropium Bromide and Albuterol Sulfate - 0781-7146-29 - (Ipratropium Bromide and Albuterol Sulfate)
Drug Information of Ipratropium Bromide and Albuterol Sulfate
| Product NDC: | 0781-7146 |
| 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: | 0781-7146 |
| Labeler Name: | Sandoz Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA202496 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130520 |
Package Information of Ipratropium Bromide and Albuterol Sulfate
| Package NDC: | 0781-7146-29 |
| Package Description: | 12 POUCH in 1 CARTON (0781-7146-29) > 5 AMPULE in 1 POUCH (0781-7146-51) > 3 mL in 1 AMPULE |
NDC Information of Ipratropium Bromide and Albuterol Sulfate
| NDC Code | 0781-7146-29 |
| Proprietary Name | Ipratropium Bromide and Albuterol Sulfate |
| Package Description | 12 POUCH in 1 CARTON (0781-7146-29) > 5 AMPULE in 1 POUCH (0781-7146-51) > 3 mL in 1 AMPULE |
| Product NDC | 0781-7146 |
| 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 | 20130520 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz 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] |
