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"68788-6839-2" National Drug Code (NDC)
Benzonatate 20 CAPSULE in 1 BOTTLE (68788-6839-2)
(Preferred Pharmaceuticals Inc.)
NDC Code
68788-6839-2
Package Description
20 CAPSULE in 1 BOTTLE (68788-6839-2)
Product NDC
68788-6839
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Benzonatate
Non-Proprietary Name
Benzonatate
Dosage Form
CAPSULE
Usage
ORAL
Start Marketing Date
20161205
Marketing Category Name
ANDA
Application Number
ANDA202765
Manufacturer
Preferred Pharmaceuticals 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/68788-6839-2