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"62959-750-74" National Drug Code (NDC)
Ibuprofen 1 BOTTLE in 1 CARTON (62959-750-74) > 100 TABLET, FILM COATED in 1 BOTTLE
(ULTRAtab Laboratories, Inc.)
NDC Code
62959-750-74
Package Description
1 BOTTLE in 1 CARTON (62959-750-74) > 100 TABLET, FILM COATED in 1 BOTTLE
Product NDC
62959-750
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Ibuprofen
Non-Proprietary Name
Ibuprofen 200mg
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20191212
Marketing Category Name
ANDA
Application Number
ANDA209076
Manufacturer
ULTRAtab Laboratories, Inc.
Substance Name
IBUPROFEN
Strength
200
Strength Unit
mg/1
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/62959-750-74