loratadine
Generic: loratadine
Labeler: walgreens co.Drug Facts
Product Profile
Brand Name
loratadine
Generic Name
loratadine
Labeler
walgreens co.
Dosage Form
TABLET, CHEWABLE
Routes
Active Ingredients
loratadine 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0363-9994
Product ID
0363-9994_7aeb3f5b-33c7-4cf8-b6ab-5f3d211ea27c
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA210088
Listing Expiration
2026-12-31
Marketing Start
2020-08-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
03639994
Hyphenated Format
0363-9994
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
loratadine (source: ndc)
Generic Name
loratadine (source: ndc)
Application Number
ANDA210088 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 3 BLISTER PACK in 1 CARTON (0363-9994-30) / 10 TABLET, CHEWABLE in 1 BLISTER PACK
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7aeb3f5b-33c7-4cf8-b6ab-5f3d211ea27c", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["665078"], "spl_set_id": ["71adc5b3-3a91-4a1f-acb3-78922a7d9d5a"], "manufacturer_name": ["WALGREENS CO."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (0363-9994-30) / 10 TABLET, CHEWABLE in 1 BLISTER PACK", "package_ndc": "0363-9994-30", "marketing_start_date": "20200801"}], "brand_name": "Loratadine", "product_id": "0363-9994_7aeb3f5b-33c7-4cf8-b6ab-5f3d211ea27c", "dosage_form": "TABLET, CHEWABLE", "product_ndc": "0363-9994", "generic_name": "Loratadine", "labeler_name": "WALGREENS CO.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loratadine", "active_ingredients": [{"name": "LORATADINE", "strength": "5 mg/1"}], "application_number": "ANDA210088", "marketing_category": "ANDA", "marketing_start_date": "20200801", "listing_expiration_date": "20261231"}