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"61919-296-30" National Drug Code (NDC)
Hydrocodone Bitartrate 30 TABLET, COATED in 1 BOTTLE (61919-296-30)
(DIRECT RX)
NDC Code
61919-296-30
Package Description
30 TABLET, COATED in 1 BOTTLE (61919-296-30)
Product NDC
61919-296
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Hydrocodone Bitartrate
Non-Proprietary Name
Hydrocodone Bitartrate
Dosage Form
TABLET, COATED
Usage
ORAL
Start Marketing Date
20140101
Marketing Category Name
ANDA
Application Number
ANDA077723
Manufacturer
DIRECT RX
Substance Name
HYDROCODONE BITARTRATE; IBUPROFEN
Strength
7.5; 200
Strength Unit
mg/1; mg/1
Pharmacy Classes
Opioid Agonist [EPC],Opioid Agonists [MoA],Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-296-30