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"37808-183-83" National Drug Code (NDC)
Rx Act Ibuprofen 225 TABLET, FILM COATED in 1 BOTTLE (37808-183-83)
(H E B)
NDC Code
37808-183-83
Package Description
225 TABLET, FILM COATED in 1 BOTTLE (37808-183-83)
Product NDC
37808-183
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Rx Act Ibuprofen
Non-Proprietary Name
Ibuprofen
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
19940204
Marketing Category Name
ANDA
Application Number
ANDA077349
Manufacturer
H E B
Substance Name
IBUPROFEN
Strength
200
Strength Unit
mg/1
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/37808-183-83