loratadine

Generic: loratadine

Labeler: atlantic biologicals corp.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name loratadine
Generic Name loratadine
Labeler atlantic biologicals corp.
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

loratadine 5 mg/5mL

Manufacturer
ATLANTIC BIOLOGICALS CORP.

Identifiers & Regulatory

Product NDC 17856-0557
Product ID 17856-0557_4bc0edf7-fe2e-d8ab-e063-6394a90a8886
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA077421
Listing Expiration 2027-12-31
Marketing Start 2019-02-13

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 178560557
Hyphenated Format 17856-0557

Supplemental Identifiers

RxCUI
692783
UNII
7AJO3BO7QN

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 ANDA077421 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/5mL
source: ndc
Packaging
  • NDC 17856-0557-1 image description image description
source: label

Packages (0)

No package records.

Ingredients (1)

loratadine (5 mg/5mL)

Linked Drug Pages (1)

Loratadine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4bc0edf7-fe2e-d8ab-e063-6394a90a8886", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["692783"], "spl_set_id": ["999a1080-5bbd-4027-b6e7-a90a6941ee27"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [], "brand_name": "Loratadine", "product_id": "17856-0557_4bc0edf7-fe2e-d8ab-e063-6394a90a8886", "dosage_form": "SOLUTION", "product_ndc": "17856-0557", "generic_name": "Loratadine", "labeler_name": "ATLANTIC BIOLOGICALS CORP.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loratadine", "active_ingredients": [{"name": "LORATADINE", "strength": "5 mg/5mL"}], "application_number": "ANDA077421", "marketing_category": "ANDA", "marketing_start_date": "20190213", "listing_expiration_date": "20271231"}