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VENTOLINHFA
VENTOLINHFA - 52125-462-01 - (albuterol sulfate)
Drug Information of VENTOLINHFA
| Product NDC: | 52125-462 |
| Proprietary Name: | VENTOLINHFA |
| Non Proprietary Name: | albuterol sulfate |
| Active Ingredient(s): | 90 ug/1 & nbsp; albuterol sulfate |
| Administration Route(s): | RESPIRATORY (INHALATION) |
| Dosage Form(s): | AEROSOL, METERED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of VENTOLINHFA
| Product NDC: | 52125-462 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020983 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20130610 |
Package Information of VENTOLINHFA
| Package NDC: | 52125-462-01 |
| Package Description: | 60 AEROSOL, METERED in 1 INHALER (52125-462-01) |
NDC Information of VENTOLINHFA
| NDC Code | 52125-462-01 |
| Proprietary Name | VENTOLINHFA |
| Package Description | 60 AEROSOL, METERED in 1 INHALER (52125-462-01) |
| Product NDC | 52125-462 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | albuterol sulfate |
| Dosage Form Name | AEROSOL, METERED |
| Route Name | RESPIRATORY (INHALATION) |
| Start Marketing Date | 20130610 |
| Marketing Category Name | NDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | ALBUTEROL SULFATE |
| Strength Number | 90 |
| Strength Unit | ug/1 |
| Pharmaceutical Classes | Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC] |
