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"79903-005-10" National Drug Code (NDC)
All Day Pain Relief 1 BOTTLE, PLASTIC in 1 CARTON (79903-005-10) / 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
(WALMART INC.)
NDC Code
79903-005-10
Package Description
1 BOTTLE, PLASTIC in 1 CARTON (79903-005-10) / 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product NDC
79903-005
Product Type Name
HUMAN OTC DRUG
Proprietary Name
All Day Pain Relief
Non-Proprietary Name
Naproxen Sodium
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20201022
Marketing Category Name
ANDA
Application Number
ANDA204872
Manufacturer
WALMART INC.
Substance Name
NAPROXEN SODIUM
Strength
220
Strength Unit
mg/1
Pharmacy Classes
Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/79903-005-10