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"43598-009-25" National Drug Code (NDC)
Guaifenesin 1200 Mg 2 BLISTER PACK in 1 CARTON (43598-009-25) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (43598-009-74)
(Dr. Reddy's Laboratories Inc.)
NDC Code
43598-009-25
Package Description
2 BLISTER PACK in 1 CARTON (43598-009-25) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (43598-009-74)
Product NDC
43598-009
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Guaifenesin 1200 Mg
Non-Proprietary Name
Guaifenesin
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20220315
Marketing Category Name
ANDA
Application Number
ANDA215932
Manufacturer
Dr. Reddy's 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/43598-009-25