Loratadine

Generic: Loratadine

Labeler: ATLANTIC BIOLOGICALS CORP.
NDC Directory HUMAN OTC DRUG ANDA Active

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

Identifiers & Regulatory

Product NDC 17856-0557
Product ID 17856-0557_34f57090-88ba-723c-e063-6294a90a36d4
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA077421
Listing Expiration 2026-12-31
Marketing Start 2019-02-13

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 178560557
Hyphenated Format 17856-0557

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
  • 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0557-1) / 5 mL in 1 CUP, UNIT-DOSE (17856-0557-2)
source: ndc

Packages (1)

17856-0557-1 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0557-1) / 5 mL in 1 CUP, UNIT-DOSE (17856-0557-2)

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": "34f57090-88ba-723c-e063-6294a90a36d4", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["692783"], "spl_set_id": ["999a1080-5bbd-4027-b6e7-a90a6941ee27"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [{"sample": false, "description": "72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0557-1)  / 5 mL in 1 CUP, UNIT-DOSE (17856-0557-2)", "package_ndc": "17856-0557-1", "marketing_start_date": "20240514"}], "brand_name": "Loratadine", "product_id": "17856-0557_34f57090-88ba-723c-e063-6294a90a36d4", "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": "20261231"}