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"10135-696-12" National Drug Code (NDC)
Alendronate 3 BLISTER PACK in 1 CARTON (10135-696-12) > 4 TABLET in 1 BLISTER PACK
(Marlex Pharmaceuticals Inc)
NDC Code
10135-696-12
Package Description
3 BLISTER PACK in 1 CARTON (10135-696-12) > 4 TABLET in 1 BLISTER PACK
Product NDC
10135-696
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Alendronate
Non-Proprietary Name
Alendronate Sodium
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20200301
Marketing Category Name
ANDA
Application Number
ANDA090258
Manufacturer
Marlex Pharmaceuticals Inc
Substance Name
ALENDRONATE SODIUM
Strength
35
Strength Unit
mg/1
Pharmacy Classes
Bisphosphonate [EPC],Diphosphonates [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/10135-696-12