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"51660-070-41" National Drug Code (NDC)
Guaifenesin 2 BLISTER PACK in 1 CARTON (51660-070-41) > 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
(OHM LABORATORIES INC)
NDC Code
51660-070-41
Package Description
2 BLISTER PACK in 1 CARTON (51660-070-41) > 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC
51660-070
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Guaifenesin
Non-Proprietary Name
Guaifenesin
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20180108
Marketing Category Name
NDA
Application Number
NDA021282
Manufacturer
OHM LABORATORIES INC
Substance Name
GUAIFENESIN
Strength
600
Strength Unit
mg/1
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51660-070-41