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"71205-898-11" National Drug Code (NDC)
Albuterol 1000 TABLET in 1 BOTTLE (71205-898-11)
(Proficient Rx LP)
NDC Code
71205-898-11
Package Description
1000 TABLET in 1 BOTTLE (71205-898-11)
Product NDC
71205-898
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Albuterol
Non-Proprietary Name
Albuterol
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20180629
Marketing Category Name
ANDA
Application Number
ANDA207046
Manufacturer
Proficient Rx LP
Substance Name
ALBUTEROL SULFATE
Strength
2
Strength Unit
mg/1
Pharmacy Classes
Adrenergic beta2-Agonists [MoA], beta2-Adrenergic Agonist [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71205-898-11