NDC 62756-277

Arformoterol Tartrate

Arformoterol Tartrate

Arformoterol Tartrate is a Respiratory (inhalation) Solution in the Human Prescription Drug category. It is labeled and distributed by Sun Pharmaceutical Industries, Inc.. The primary component is Arformoterol Tartrate.

Product ID62756-277_9d97f601-a41c-48b7-8ba0-27bc75500e06
NDC62756-277
Product TypeHuman Prescription Drug
Proprietary NameArformoterol Tartrate
Generic NameArformoterol Tartrate
Dosage FormSolution
Route of AdministrationRESPIRATORY (INHALATION)
Marketing Start Date2022-05-28
Marketing CategoryANDA /
Application NumberANDA215385
Labeler NameSun Pharmaceutical Industries, Inc.
Substance NameARFORMOTEROL TARTRATE
Active Ingredient Strength15 ug/2mL
Pharm ClassesAdrenergic beta2-Agonists [MoA], beta2-Adrenergic Agonist [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 62756-277-02

6 POUCH in 1 CARTON (62756-277-02) > 5 VIAL, SINGLE-DOSE in 1 POUCH > 2 mL in 1 VIAL, SINGLE-DOSE
Marketing Start Date2022-05-28
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Arformoterol Tartrate" or generic name "Arformoterol Tartrate"

NDCBrand NameGeneric Name
0093-5955Arformoterol tartrateArformoterol tartrate
62332-633Arformoterol tartrateArformoterol tartrate
62756-277Arformoterol TartrateArformoterol Tartrate
68462-833ARFORMOTEROL TARTRATEarformoterol tartrate
69097-168arformoterol tartratearformoterol tartrate
70748-175Arformoterol tartrateArformoterol tartrate
70748-257Arformoterol TartrateArformoterol Tartrate
70756-612arformoterol tartratearformoterol tartrate
63402-911Brovanaarformoterol tartrate

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.