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"51660-724-69" National Drug Code (NDC)
Loratadine And Pseudoephedrine 1 BLISTER PACK in 1 CARTON (51660-724-69) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
(Ohm Laboratories Inc.)
NDC Code
51660-724-69
Package Description
1 BLISTER PACK in 1 CARTON (51660-724-69) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC
51660-724
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Loratadine And Pseudoephedrine
Non-Proprietary Name
Loratadine And Pseudoephedrine
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20041117
Marketing Category Name
ANDA
Application Number
ANDA076557
Manufacturer
Ohm Laboratories Inc.
Substance Name
LORATADINE; PSEUDOEPHEDRINE SULFATE
Strength
10; 240
Strength Unit
mg/1; mg/1
Pharmacy Classes
Adrenergic alpha-Agonists [MoA], alpha-Adrenergic Agonist [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51660-724-69