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"51672-1301-0" National Drug Code (NDC)

Ammonium Lactate 385 g in 1 BOTTLE, PLASTIC (51672-1301-0)
(Sun Pharmaceutical Industries, Inc.)

NDC Code51672-1301-0
Package Description385 g in 1 BOTTLE, PLASTIC (51672-1301-0)
Product NDC51672-1301
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmmonium Lactate
Non-Proprietary NameAmmonium Lactate
Dosage FormCREAM
UsageTOPICAL
Start Marketing Date20030410
Marketing Category NameANDA
Application NumberANDA075883
ManufacturerSun Pharmaceutical Industries, Inc.
Substance NameAMMONIUM LACTATE
Strength120
Strength Unitmg/g
Pharmacy ClassesAcidifying Activity [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51672-1301-0





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