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IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE
IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE - 76204-600-01 - (Ipratropium Bromide and Albuterol Sulfate)
Drug Information of IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE
| Product NDC: | 76204-600 |
| 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: | 76204-600 |
| Labeler Name: | Ritedose Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA202496 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121015 |
Package Information of IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE
| Package NDC: | 76204-600-01 |
| Package Description: | 30 POUCH in 1 CARTON (76204-600-01) > 1 AMPULE in 1 POUCH > 3 mL in 1 AMPULE |
NDC Information of IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE
| NDC Code | 76204-600-01 |
| Proprietary Name | IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE |
| Package Description | 30 POUCH in 1 CARTON (76204-600-01) > 1 AMPULE in 1 POUCH > 3 mL in 1 AMPULE |
| Product NDC | 76204-600 |
| 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 | 20121015 |
| Marketing Category Name | ANDA |
| Labeler Name | Ritedose Pharmaceuticals, LLC |
| 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] |
