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"51079-871-19" National Drug Code (NDC)
Sucralfate 25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-871-19) > 1 TABLET in 1 BLISTER PACK (51079-871-17)
(UDL Laboratories, Inc.)
NDC Code
51079-871-19
Package Description
25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-871-19) > 1 TABLET in 1 BLISTER PACK (51079-871-17)
Product NDC
51079-871
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Sucralfate
Non-Proprietary Name
Sucralfate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20110527
Marketing Category Name
ANDA
Application Number
ANDA070848
Manufacturer
UDL Laboratories, Inc.
Substance Name
SUCRALFATE
Strength
1
Strength Unit
g/1
Pharmacy Classes
Aluminum Complex [EPC],Organometallic Compounds [Chemical/Ingredient]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51079-871-19