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"68788-7250-2" National Drug Code (NDC)
Glipizide 20 TABLET in 1 BOTTLE, PLASTIC (68788-7250-2)
(Preferred Pharmaceuticals Inc.)
NDC Code
68788-7250-2
Package Description
20 TABLET in 1 BOTTLE, PLASTIC (68788-7250-2)
Product NDC
68788-7250
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Glipizide
Non-Proprietary Name
Glipizide
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20180827
Marketing Category Name
ANDA
Application Number
ANDA074223
Manufacturer
Preferred Pharmaceuticals Inc.
Substance Name
GLIPIZIDE
Strength
10
Strength Unit
mg/1
Pharmacy Classes
Sulfonylurea [EPC],Sulfonylurea Compounds [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68788-7250-2