loratadine

Generic: loratadine

Labeler: st. mary's medical park pharmacy
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name loratadine
Generic Name loratadine
Labeler st. mary's medical park pharmacy
Dosage Form TABLET
Routes
ORAL
Active Ingredients

loratadine 10 mg/1

Manufacturer
ST. MARY'S MEDICAL PARK PHARMACY

Identifiers & Regulatory

Product NDC 60760-609
Product ID 60760-609_0cca91d6-0bce-a81c-e063-6294a90a2613
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA210722
Listing Expiration 2026-12-31
Marketing Start 2022-07-31

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60760609
Hyphenated Format 60760-609

Supplemental Identifiers

RxCUI
311372
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 ANDA210722 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (60760-609-00)
source: ndc

Packages (1)

Ingredients (1)

loratadine (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0cca91d6-0bce-a81c-e063-6294a90a2613", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["311372"], "spl_set_id": ["0cca8170-dd10-3840-e063-6394a90ab243"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (60760-609-00)", "package_ndc": "60760-609-00", "marketing_start_date": "20230330"}], "brand_name": "LORATADINE", "product_id": "60760-609_0cca91d6-0bce-a81c-e063-6294a90a2613", "dosage_form": "TABLET", "product_ndc": "60760-609", "generic_name": "LORATADINE", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "LORATADINE", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "ANDA210722", "marketing_category": "ANDA", "marketing_start_date": "20220731", "listing_expiration_date": "20261231"}