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"70518-3917-0" National Drug Code (NDC)
Dicyclomine Hydrochloride 30 TABLET in 1 BLISTER PACK (70518-3917-0)
(REMEDYREPACK INC.)
NDC Code
70518-3917-0
Package Description
30 TABLET in 1 BLISTER PACK (70518-3917-0)
Product NDC
70518-3917
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Dicyclomine Hydrochloride
Non-Proprietary Name
Dicyclomine Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20231119
Marketing Category Name
ANDA
Application Number
ANDA216782
Manufacturer
REMEDYREPACK INC.
Substance Name
DICYCLOMINE HYDROCHLORIDE
Strength
20
Strength Unit
mg/1
Pharmacy Classes
Anticholinergic [EPC], Cholinergic Antagonists [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-3917-0