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"51079-746-19" National Drug Code (NDC)
Diltiazem Hydrochloride 25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-746-19) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-746-17)
(Mylan Institutional Inc.)
NDC Code
51079-746-19
Package Description
25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-746-19) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-746-17)
Product NDC
51079-746
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Diltiazem Hydrochloride
Non-Proprietary Name
Diltiazem Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
19960307
Marketing Category Name
ANDA
Application Number
ANDA072838
Manufacturer
Mylan Institutional Inc.
Substance Name
DILTIAZEM HYDROCHLORIDE
Strength
60
Strength Unit
mg/1
Pharmacy Classes
Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51079-746-19