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"0597-0039-37" National Drug Code (NDC)
Micardis 3 BLISTER PACK in 1 CARTON (0597-0039-37) / 10 TABLET in 1 BLISTER PACK
(Boehringer Ingelheim Pharmaceuticals, Inc.)
NDC Code
0597-0039-37
Package Description
3 BLISTER PACK in 1 CARTON (0597-0039-37) / 10 TABLET in 1 BLISTER PACK
Product NDC
0597-0039
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Micardis
Non-Proprietary Name
Telmisartan
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20001201
End Marketing Date
20250430
Marketing Category Name
NDA
Application Number
NDA020850
Manufacturer
Boehringer Ingelheim Pharmaceuticals, Inc.
Substance Name
TELMISARTAN
Strength
20
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/0597-0039-37