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Albuterol - albuterol

Navigation: NDC > Supplier starting with: U > UDL LABORATORIES, INC.
Field Value
NDC Code: 51079-657
Proprietary Name: Albuterol
Suffix:
Non-Proprietary Name: albuterol
Dosage Form: TABLET
Method: ORAL
Original Marketing Date: 12-08-2011
Category Name: ANDA
Application Number: ANDA072894
Labeler: UDL LABORATORIES, INC.
Substance Name: ALBUTEROL SULFATE
Active Numerator Strength: 2
Active Ingredient Unit: mg/1
Pharm Classes: Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]
DEA Schedule: