up and up allergy relief

Generic: loratadine

Labeler: target corporation
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name up and up allergy relief
Generic Name loratadine
Labeler target corporation
Dosage Form TABLET
Routes
ORAL
Active Ingredients

loratadine 10 mg/1

Manufacturer
Target Corporation

Identifiers & Regulatory

Product NDC 11673-612
Product ID 11673-612_244b9b86-cddc-46fb-8f03-312a3fed96d1
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA076301
Listing Expiration 2026-12-31
Marketing Start 2012-03-26

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 11673612
Hyphenated Format 11673-612

Supplemental Identifiers

RxCUI
311372
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 up and up allergy relief (source: ndc)
Generic Name loratadine (source: ndc)
Application Number ANDA076301 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (11673-612-03) / 70 TABLET in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (11673-612-65) / 30 TABLET in 1 BOTTLE
  • 100 TABLET in 1 BOTTLE (11673-612-78)
  • 1 BOTTLE in 1 CARTON (11673-612-82) / 200 TABLET in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (11673-612-87) / 300 TABLET in 1 BOTTLE
source: ndc

Packages (5)

11673-612-03 1 BOTTLE in 1 CARTON (11673-612-03) / 70 TABLET in 1 BOTTLE 11673-612-65 1 BOTTLE in 1 CARTON (11673-612-65) / 30 TABLET in 1 BOTTLE 11673-612-78 100 TABLET in 1 BOTTLE (11673-612-78) 11673-612-82 1 BOTTLE in 1 CARTON (11673-612-82) / 200 TABLET in 1 BOTTLE 11673-612-87 1 BOTTLE in 1 CARTON (11673-612-87) / 300 TABLET in 1 BOTTLE

Ingredients (1)

loratadine (10 mg/1)

Linked Drug Pages (1)

up and up allergy relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "244b9b86-cddc-46fb-8f03-312a3fed96d1", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["311372"], "spl_set_id": ["c4ef0110-89c3-4ded-9a9a-75c0f794f869"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-612-03)  / 70 TABLET in 1 BOTTLE", "package_ndc": "11673-612-03", "marketing_start_date": "20150219"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-612-65)  / 30 TABLET in 1 BOTTLE", "package_ndc": "11673-612-65", "marketing_start_date": "20120412"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (11673-612-78)", "package_ndc": "11673-612-78", "marketing_start_date": "20150320"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-612-82)  / 200 TABLET in 1 BOTTLE", "package_ndc": "11673-612-82", "marketing_start_date": "20120412"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-612-87)  / 300 TABLET in 1 BOTTLE", "package_ndc": "11673-612-87", "marketing_start_date": "20160315"}], "brand_name": "up and up allergy relief", "product_id": "11673-612_244b9b86-cddc-46fb-8f03-312a3fed96d1", "dosage_form": "TABLET", "product_ndc": "11673-612", "generic_name": "Loratadine", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "up and up allergy relief", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "ANDA076301", "marketing_category": "ANDA", "marketing_start_date": "20120326", "listing_expiration_date": "20261231"}