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"70518-0652-2" National Drug Code (NDC)
Buprenorphine Hydrochloride Sublingual 30 TABLET in 1 BOTTLE, PLASTIC (70518-0652-2)
(REMEDYREPACK INC.)
NDC Code
70518-0652-2
Package Description
30 TABLET in 1 BOTTLE, PLASTIC (70518-0652-2)
Product NDC
70518-0652
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Buprenorphine Hydrochloride Sublingual
Non-Proprietary Name
Buprenorphine Hydrochloride Sublingual
Dosage Form
TABLET
Usage
SUBLINGUAL
Start Marketing Date
20170731
Marketing Category Name
ANDA
Application Number
ANDA201066
Manufacturer
REMEDYREPACK INC.
Substance Name
BUPRENORPHINE HYDROCHLORIDE
Strength
2
Strength Unit
mg/1
Pharmacy Classes
Partial Opioid Agonists [MoA],Partial Opioid Agonist [EPC]
DEA Schedule
CIII
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-0652-2