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"68462-199-13" National Drug Code (NDC)
Telmisartan 3 BLISTER PACK in 1 CARTON (68462-199-13) / 10 TABLET in 1 BLISTER PACK
(Glenmark Pharmaceuticals Inc., USA)
NDC Code
68462-199-13
Package Description
3 BLISTER PACK in 1 CARTON (68462-199-13) / 10 TABLET in 1 BLISTER PACK
Product NDC
68462-199
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Telmisartan
Non-Proprietary Name
Telmisartan
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20140707
Marketing Category Name
ANDA
Application Number
ANDA090032
Manufacturer
Glenmark Pharmaceuticals Inc., USA
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/68462-199-13