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"62207-839-72" National Drug Code (NDC)
Guaifenesin 9 BLISTER PACK in 1 CARTON (62207-839-72) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
(Granules India Ltd)
NDC Code
62207-839-72
Package Description
9 BLISTER PACK in 1 CARTON (62207-839-72) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC
62207-839
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Guaifenesin
Non-Proprietary Name
Guaifenesin
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20201218
Marketing Category Name
ANDA
Application Number
ANDA213420
Manufacturer
Granules India Ltd
Substance Name
GUAIFENESIN
Strength
600
Strength Unit
mg/1
Pharmacy Classes
Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/62207-839-72