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Product NDC
37205-650
11-digit product format
372050650
Labeler code
37205
Product ID
37205-650_03064053-2b8d-46ce-9115-493f7b5a4f0b
Type
HUMAN OTC DRUG
Nonproprietary name
fexofenadine hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Cardinal Health
Application
ANDA076447
Marketing category
ANDA
Marketing start
2011-05-16
Marketing end
2019-04-01
Substance
FEXOFENADINE HY
Active strength
180 mg/1
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
37205-650-65EA - Each37205-65046876273-fe03-419b-8f33-b1130ad0dbad12012-07-24
37205-650-72EA - Each37205-650f21c38c2-ab03-4d30-b905-f0d6ad89239012014-07-02
37205-650-88EA - Each37205-650ae7ef821-8994-4052-bde3-afd2faea3fe912012-07-24