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"70518-2572-0" National Drug Code (NDC)
Telmisartan 3 BLISTER PACK in 1 CARTON (70518-2572-0) / 10 TABLET in 1 BLISTER PACK
(REMEDYREPACK INC.)
NDC Code
70518-2572-0
Package Description
3 BLISTER PACK in 1 CARTON (70518-2572-0) / 10 TABLET in 1 BLISTER PACK
Product NDC
70518-2572
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Telmisartan
Non-Proprietary Name
Telmisartan
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20200210
Marketing Category Name
ANDA
Application Number
ANDA090032
Manufacturer
REMEDYREPACK INC.
Substance Name
TELMISARTAN
Strength
80
Strength Unit
mg/1
Pharmacy Classes
Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-2572-0