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"57664-134-13" National Drug Code (NDC)
Benzonatate 500 CAPSULE in 1 BOTTLE (57664-134-13)
(Sun Pharmaceutical Industries, Inc.)
NDC Code
57664-134-13
Package Description
500 CAPSULE in 1 BOTTLE (57664-134-13)
Product NDC
57664-134
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Benzonatate
Non-Proprietary Name
Benzonatate
Dosage Form
CAPSULE
Usage
ORAL
Start Marketing Date
20080407
Marketing Category Name
ANDA
Application Number
ANDA040587
Manufacturer
Sun Pharmaceutical Industries, Inc.
Substance Name
BENZONATATE
Strength
200
Strength Unit
mg/1
Pharmacy Classes
Decreased Tracheobronchial Stretch Receptor Activity [PE],Non-narcotic Antitussive [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/57664-134-13