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Albuterol
Albuterol - 21695-198-01 - (Albuterol)
Drug Information of Albuterol
| Product NDC: | 21695-198 |
| Proprietary Name: | Albuterol |
| Non Proprietary Name: | Albuterol |
| Active Ingredient(s): | 90 ug/1 & nbsp; Albuterol |
| Administration Route(s): | ORAL |
| Dosage Form(s): | AEROSOL, METERED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Albuterol
| Product NDC: | 21695-198 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA072273 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19960814 |
Package Information of Albuterol
| Package NDC: | 21695-198-01 |
| Package Description: | 200 AEROSOL, METERED in 1 CANISTER (21695-198-01) |
NDC Information of Albuterol
| NDC Code | 21695-198-01 |
| Proprietary Name | Albuterol |
| Package Description | 200 AEROSOL, METERED in 1 CANISTER (21695-198-01) |
| Product NDC | 21695-198 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Albuterol |
| Dosage Form Name | AEROSOL, METERED |
| Route Name | ORAL |
| Start Marketing Date | 19960814 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | ALBUTEROL |
| Strength Number | 90 |
| Strength Unit | ug/1 |
| Pharmaceutical Classes | Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC] |
