wal-fex
Generic: fexofenadine hydrochloride
Labeler: walgreens companyDrug Facts
Product Profile
Brand Name
wal-fex
Generic Name
fexofenadine hydrochloride
Labeler
walgreens company
Dosage Form
TABLET
Routes
Active Ingredients
fexofenadine hydrochloride 180 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0363-0784
Product ID
0363-0784_7e7ffc3e-e6f3-18ec-ed27-f9268790597e
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA076502
Listing Expiration
2026-12-31
Marketing Start
2011-04-13
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
03630784
Hyphenated Format
0363-0784
Supplemental Identifiers
RxCUI
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
wal-fex (source: ndc)
Generic Name
fexofenadine hydrochloride (source: ndc)
Application Number
ANDA076502 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 180 mg/1
Packaging
- 1 BLISTER PACK in 1 CARTON (0363-0784-07) / 5 TABLET in 1 BLISTER PACK
- 1 BOTTLE in 1 CARTON (0363-0784-15) / 150 TABLET in 1 BOTTLE
- 180 TABLET in 1 BOTTLE (0363-0784-18)
- 3 BLISTER PACK in 1 CARTON (0363-0784-29) / 5 TABLET in 1 BLISTER PACK
- 1 BOTTLE in 1 CARTON (0363-0784-30) / 30 TABLET in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (0363-0784-40) / 40 TABLET in 1 BOTTLE
- 2 BOTTLE in 1 CARTON (0363-0784-43) / 30 TABLET in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (0363-0784-45) / 45 TABLET in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (0363-0784-75) / 70 TABLET in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (0363-0784-90) / 90 TABLET in 1 BOTTLE
Packages (10)
0363-0784-07
1 BLISTER PACK in 1 CARTON (0363-0784-07) / 5 TABLET in 1 BLISTER PACK
0363-0784-15
1 BOTTLE in 1 CARTON (0363-0784-15) / 150 TABLET in 1 BOTTLE
0363-0784-18
180 TABLET in 1 BOTTLE (0363-0784-18)
0363-0784-29
3 BLISTER PACK in 1 CARTON (0363-0784-29) / 5 TABLET in 1 BLISTER PACK
0363-0784-30
1 BOTTLE in 1 CARTON (0363-0784-30) / 30 TABLET in 1 BOTTLE
0363-0784-40
1 BOTTLE in 1 CARTON (0363-0784-40) / 40 TABLET in 1 BOTTLE
0363-0784-43
2 BOTTLE in 1 CARTON (0363-0784-43) / 30 TABLET in 1 BOTTLE
0363-0784-45
1 BOTTLE in 1 CARTON (0363-0784-45) / 45 TABLET in 1 BOTTLE
0363-0784-75
1 BOTTLE in 1 CARTON (0363-0784-75) / 70 TABLET in 1 BOTTLE
0363-0784-90
1 BOTTLE in 1 CARTON (0363-0784-90) / 90 TABLET in 1 BOTTLE
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7e7ffc3e-e6f3-18ec-ed27-f9268790597e", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420", "1116528"], "spl_set_id": ["95d420ea-6337-304f-54c3-0c75be1608e2"], "manufacturer_name": ["Walgreens Company"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (0363-0784-07) / 5 TABLET in 1 BLISTER PACK", "package_ndc": "0363-0784-07", "marketing_start_date": "20110413"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-0784-15) / 150 TABLET in 1 BOTTLE", "package_ndc": "0363-0784-15", "marketing_start_date": "20110413"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (0363-0784-18)", "package_ndc": "0363-0784-18", "marketing_start_date": "20220713"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (0363-0784-29) / 5 TABLET in 1 BLISTER PACK", "package_ndc": "0363-0784-29", "marketing_start_date": "20110413"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-0784-30) / 30 TABLET in 1 BOTTLE", "package_ndc": "0363-0784-30", "marketing_start_date": "20110413"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-0784-40) / 40 TABLET in 1 BOTTLE", "package_ndc": "0363-0784-40", "marketing_start_date": "20110413"}, {"sample": false, "description": "2 BOTTLE in 1 CARTON (0363-0784-43) / 30 TABLET in 1 BOTTLE", "package_ndc": "0363-0784-43", "marketing_start_date": "20110413"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-0784-45) / 45 TABLET in 1 BOTTLE", "package_ndc": "0363-0784-45", "marketing_start_date": "20110413"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-0784-75) / 70 TABLET in 1 BOTTLE", "package_ndc": "0363-0784-75", "marketing_start_date": "20110413"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-0784-90) / 90 TABLET in 1 BOTTLE", "package_ndc": "0363-0784-90", "marketing_start_date": "20110413"}], "brand_name": "Wal-Fex", "product_id": "0363-0784_7e7ffc3e-e6f3-18ec-ed27-f9268790597e", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0363-0784", "generic_name": "Fexofenadine hydrochloride", "labeler_name": "Walgreens Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Wal-Fex", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA076502", "marketing_category": "ANDA", "marketing_start_date": "20110413", "listing_expiration_date": "20261231"}