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"10135-763-90" National Drug Code (NDC)
Loratadine Allergy Relief 90 TABLET in 1 BOTTLE (10135-763-90)
(Marlex Pharmaceuticals, Inc.)
NDC Code
10135-763-90
Package Description
90 TABLET in 1 BOTTLE (10135-763-90)
Product NDC
10135-763
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Loratadine Allergy Relief
Non-Proprietary Name
Loratadine
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20221001
Marketing Category Name
ANDA
Application Number
ANDA076134
Manufacturer
Marlex Pharmaceuticals, Inc.
Substance Name
LORATADINE
Strength
10
Strength Unit
mg/1
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/10135-763-90