loratadine

Generic: loratadine

Labeler: walgreens company
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name loratadine
Generic Name loratadine
Labeler walgreens company
Dosage Form TABLET
Routes
ORAL
Active Ingredients

loratadine 5 mg/1

Manufacturer
Walgreens Company

Identifiers & Regulatory

Product NDC 0363-9955
Product ID 0363-9955_c3c18e2a-3dba-eeae-c893-0b3ab6a512c0
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA212795
Listing Expiration 2026-12-31
Marketing Start 2021-05-19

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03639955
Hyphenated Format 0363-9955

Supplemental Identifiers

RxCUI
672558
UNII
7AJO3BO7QN

Packaging Origin

Original Packager
true

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 ANDA212795 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 3 BLISTER PACK in 1 CARTON (0363-9955-30) / 10 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

0363-9955-30 3 BLISTER PACK in 1 CARTON (0363-9955-30) / 10 TABLET in 1 BLISTER PACK

Ingredients (1)

loratadine (5 mg/1)

Linked Drug Pages (1)

Loratadine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c3c18e2a-3dba-eeae-c893-0b3ab6a512c0", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["672558"], "spl_set_id": ["8229ca40-31cf-3dbd-078d-364f5674cb21"], "manufacturer_name": ["Walgreens Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (0363-9955-30)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "0363-9955-30", "marketing_start_date": "20230714"}], "brand_name": "Loratadine", "product_id": "0363-9955_c3c18e2a-3dba-eeae-c893-0b3ab6a512c0", "dosage_form": "TABLET", "product_ndc": "0363-9955", "generic_name": "Loratadine", "labeler_name": "Walgreens Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loratadine", "active_ingredients": [{"name": "LORATADINE", "strength": "5 mg/1"}], "application_number": "ANDA212795", "marketing_category": "ANDA", "marketing_start_date": "20210519", "listing_expiration_date": "20261231"}