loratadine
Generic: loratadine
Labeler: bionpharma inc.Drug Facts
Product Profile
Brand Name
loratadine
Generic Name
loratadine
Labeler
bionpharma inc.
Dosage Form
CAPSULE, LIQUID FILLED
Routes
Active Ingredients
loratadine 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
69452-283
Product ID
69452-283_29f9d1b7-7751-f253-e063-6394a90ac12f
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA202538
Listing Expiration
2026-12-31
Marketing Start
2020-03-20
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69452283
Hyphenated Format
69452-283
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
ANDA202538 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- Principal Display Panel 5's Carton
Packages (0)
No package records.
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "29f9d1b7-7751-f253-e063-6394a90ac12f", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["828269"], "spl_set_id": ["4fa705fb-859e-4046-b153-a8338c50a97d"], "manufacturer_name": ["Bionpharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [], "brand_name": "LORATADINE", "product_id": "69452-283_29f9d1b7-7751-f253-e063-6394a90ac12f", "dosage_form": "CAPSULE, LIQUID FILLED", "product_ndc": "69452-283", "generic_name": "LORATADINE", "labeler_name": "Bionpharma Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "LORATADINE", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "ANDA202538", "marketing_category": "ANDA", "marketing_start_date": "20200320", "listing_expiration_date": "20261231"}