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"70518-1723-0" National Drug Code (NDC)
Methocarbamol 30 TABLET, COATED in 1 BLISTER PACK (70518-1723-0)
(REMEDYREPACK INC.)
NDC Code
70518-1723-0
Package Description
30 TABLET, COATED in 1 BLISTER PACK (70518-1723-0)
Product NDC
70518-1723
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Methocarbamol
Non-Proprietary Name
Methocarbamol Tablets
Dosage Form
TABLET, COATED
Usage
ORAL
Start Marketing Date
20181210
Marketing Category Name
ANDA
Application Number
ANDA209312
Manufacturer
REMEDYREPACK INC.
Substance Name
METHOCARBAMOL
Strength
500
Strength Unit
mg/1
Pharmacy Classes
Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-1723-0