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"16714-870-02" National Drug Code (NDC)
Risedronate Sodium 1 DOSE PACK in 1 CARTON (16714-870-02) / 4 TABLET, DELAYED RELEASE in 1 DOSE PACK (16714-870-01)
(NorthStar RxLLC)
NDC Code
16714-870-02
Package Description
1 DOSE PACK in 1 CARTON (16714-870-02) / 4 TABLET, DELAYED RELEASE in 1 DOSE PACK (16714-870-01)
Product NDC
16714-870
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Risedronate Sodium
Non-Proprietary Name
Risedronate Sodium
Dosage Form
TABLET, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
20190814
End Marketing Date
20250228
Marketing Category Name
ANDA
Application Number
ANDA203925
Manufacturer
NorthStar RxLLC
Substance Name
RISEDRONATE 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/16714-870-02