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"68382-075-73" National Drug Code (NDC)
Risedronate Sodium 1 BLISTER PACK in 1 CARTON (68382-075-73) > 4 TABLET, DELAYED RELEASE in 1 BLISTER PACK
(Zydus Pharmaceuticals USA Inc.)
NDC Code
68382-075-73
Package Description
1 BLISTER PACK in 1 CARTON (68382-075-73) > 4 TABLET, DELAYED RELEASE in 1 BLISTER PACK
Product NDC
68382-075
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
20190410
Marketing Category Name
ANDA
Application Number
ANDA203822
Manufacturer
Zydus Pharmaceuticals USA Inc.
Substance Name
RISEDRONATE SODIUM ANHYDROUS
Strength
35
Strength Unit
mg/1
Pharmacy Classes
Bisphosphonate [EPC], Diphosphonates [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68382-075-73