"57664-134-13" National Drug Code (NDC)

Benzonatate 500 CAPSULE in 1 BOTTLE (57664-134-13)
(Sun Pharmaceutical Industries, Inc.)

NDC Code57664-134-13
Package Description500 CAPSULE in 1 BOTTLE (57664-134-13)
Product NDC57664-134
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBenzonatate
Non-Proprietary NameBenzonatate
Dosage FormCAPSULE
UsageORAL
Start Marketing Date20080407
Marketing Category NameANDA
Application NumberANDA040587
ManufacturerSun Pharmaceutical Industries, Inc.
Substance NameBENZONATATE
Strength200
Strength Unitmg/1
Pharmacy ClassesDecreased Tracheobronchial Stretch Receptor Activity [PE],Non-narcotic Antitussive [EPC]

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