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"47335-638-68" National Drug Code (NDC)
Alendronate Sodium 1 BLISTER PACK in 1 CARTON (47335-638-68) > 4 TABLET in 1 BLISTER PACK
(Sun Pharma Global FZE)
NDC Code
47335-638-68
Package Description
1 BLISTER PACK in 1 CARTON (47335-638-68) > 4 TABLET in 1 BLISTER PACK
Product NDC
47335-638
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Alendronate Sodium
Non-Proprietary Name
Alendronate Sodium
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20141215
Marketing Category Name
ANDA
Application Number
ANDA090022
Manufacturer
Sun Pharma Global FZE
Substance Name
ALENDRONATE SODIUM
Strength
70
Strength Unit
mg/1
Pharmacy Classes
Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/47335-638-68