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"21130-399-01" National Drug Code (NDC)
Mucus Relief Max 1 BLISTER PACK in 1 CARTON (21130-399-01) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
(Better Living Brands, LLC)
NDC Code
21130-399-01
Package Description
1 BLISTER PACK in 1 CARTON (21130-399-01) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC
21130-399
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Mucus Relief Max
Non-Proprietary Name
Guaifenesin
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20200717
Marketing Category Name
ANDA
Application Number
ANDA210453
Manufacturer
Better Living Brands, LLC
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/21130-399-01