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"68210-1220-1" National Drug Code (NDC)
Fexofenadine Hydrochloride 1 BLISTER PACK in 1 BLISTER PACK (68210-1220-1) > 4 TABLET in 1 BLISTER PACK
(Spirit Pharmaceuticals LLC)
NDC Code
68210-1220-1
Package Description
1 BLISTER PACK in 1 BLISTER PACK (68210-1220-1) > 4 TABLET in 1 BLISTER PACK
Product NDC
68210-1220
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Fexofenadine Hydrochloride
Non-Proprietary Name
Fexofenadine Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20200316
Marketing Category Name
ANDA
Application Number
ANDA210137
Manufacturer
Spirit Pharmaceuticals LLC
Substance Name
FEXOFENADINE HYDROCHLORIDE
Strength
180
Strength Unit
mg/1
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68210-1220-1