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"70518-2217-0" National Drug Code (NDC)
Buprenorphine 30 TABLET in 1 BLISTER PACK (70518-2217-0)
(REMEDYREPACK INC.)
NDC Code
70518-2217-0
Package Description
30 TABLET in 1 BLISTER PACK (70518-2217-0)
Product NDC
70518-2217
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Buprenorphine
Non-Proprietary Name
Buprenorphine
Dosage Form
TABLET
Usage
SUBLINGUAL
Start Marketing Date
20190715
Marketing Category Name
ANDA
Application Number
ANDA207276
Manufacturer
REMEDYREPACK INC.
Substance Name
BUPRENORPHINE HYDROCHLORIDE
Strength
2
Strength Unit
mg/1
Pharmacy Classes
Partial Opioid Agonist [EPC], Partial Opioid Agonists [MoA]
DEA Schedule
CIII
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-2217-0