loratadine

Generic: loratadine

Labeler: safeway inc.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name loratadine
Generic Name loratadine
Labeler safeway inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

loratadine 10 mg/1

Manufacturer
SAFEWAY INC.

Identifiers & Regulatory

Product NDC 21130-526
Product ID 21130-526_5ef0c05a-40de-40cb-b52c-3f1ab96a5348
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA076134
Listing Expiration 2026-12-31
Marketing Start 2009-06-06

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 21130526
Hyphenated Format 21130-526

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 loratadine (source: ndc)
Generic Name loratadine (source: ndc)
Application Number ANDA076134 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (21130-526-13) / 120 TABLET in 1 BOTTLE
  • 3 BLISTER PACK in 1 CARTON (21130-526-31) / 10 TABLET in 1 BLISTER PACK
  • 1 BOTTLE in 1 CARTON (21130-526-38) / 365 TABLET in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (21130-526-43) / 45 TABLET in 1 BOTTLE
  • 1 BLISTER PACK in 1 CARTON (21130-526-69) / 10 TABLET in 1 BLISTER PACK
source: ndc

Packages (5)

21130-526-13 1 BOTTLE in 1 CARTON (21130-526-13) / 120 TABLET in 1 BOTTLE 21130-526-31 3 BLISTER PACK in 1 CARTON (21130-526-31) / 10 TABLET in 1 BLISTER PACK 21130-526-38 1 BOTTLE in 1 CARTON (21130-526-38) / 365 TABLET in 1 BOTTLE 21130-526-43 1 BOTTLE in 1 CARTON (21130-526-43) / 45 TABLET in 1 BOTTLE 21130-526-69 1 BLISTER PACK in 1 CARTON (21130-526-69) / 10 TABLET in 1 BLISTER PACK

Ingredients (1)

loratadine (10 mg/1)

Linked Drug Pages (1)

Loratadine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5ef0c05a-40de-40cb-b52c-3f1ab96a5348", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["311372"], "spl_set_id": ["1092b8af-25f2-4c25-b3bc-5ffb14e96024"], "manufacturer_name": ["SAFEWAY INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (21130-526-13)  / 120 TABLET in 1 BOTTLE", "package_ndc": "21130-526-13", "marketing_start_date": "20090606"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (21130-526-31)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "21130-526-31", "marketing_start_date": "20090606"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (21130-526-38)  / 365 TABLET in 1 BOTTLE", "package_ndc": "21130-526-38", "marketing_start_date": "20090606"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (21130-526-43)  / 45 TABLET in 1 BOTTLE", "package_ndc": "21130-526-43", "marketing_start_date": "20090606"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (21130-526-69)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "21130-526-69", "marketing_start_date": "20090606"}], "brand_name": "Loratadine", "product_id": "21130-526_5ef0c05a-40de-40cb-b52c-3f1ab96a5348", "dosage_form": "TABLET", "product_ndc": "21130-526", "generic_name": "Loratadine", "labeler_name": "SAFEWAY INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loratadine", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "ANDA076134", "marketing_category": "ANDA", "marketing_start_date": "20090606", "listing_expiration_date": "20261231"}