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"51660-567-54" National Drug Code (NDC)
Guaifenesin 14 TABLET, EXTENDED RELEASE in 1 CARTON (51660-567-54)
(Ohm Laboratories, Inc.)
NDC Code
51660-567-54
Package Description
14 TABLET, EXTENDED RELEASE in 1 CARTON (51660-567-54)
Product NDC
51660-567
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Guaifenesin
Non-Proprietary Name
Guaifenesin
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20220401
Marketing Category Name
ANDA
Application Number
ANDA209254
Manufacturer
Ohm Laboratories, Inc.
Substance Name
GUAIFENESIN
Strength
1200
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/51660-567-54