loratadine allergy relief

Generic: loratadine

Labeler: heb
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name loratadine allergy relief
Generic Name loratadine
Labeler heb
Dosage Form TABLET
Routes
ORAL
Active Ingredients

loratadine 10 mg/1

Manufacturer
HEB

Identifiers & Regulatory

Product NDC 37808-529
Product ID 37808-529_c624b449-9db2-4b2e-852f-28f745aa7e2a
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA076134
Listing Expiration 2026-12-31
Marketing Start 2018-02-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 37808529
Hyphenated Format 37808-529

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 allergy relief (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
  • 100 TABLET in 1 BOTTLE (37808-529-01)
  • 1 BLISTER PACK in 1 CARTON (37808-529-11) / 10 TABLET in 1 BLISTER PACK
  • 30 BLISTER PACK in 1 CARTON (37808-529-31) / 1 TABLET in 1 BLISTER PACK
source: ndc

Packages (3)

37808-529-01 100 TABLET in 1 BOTTLE (37808-529-01) 37808-529-11 1 BLISTER PACK in 1 CARTON (37808-529-11) / 10 TABLET in 1 BLISTER PACK 37808-529-31 30 BLISTER PACK in 1 CARTON (37808-529-31) / 1 TABLET in 1 BLISTER PACK

Ingredients (1)

loratadine (10 mg/1)

Linked Drug Pages (1)

Loratadine Allergy Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c624b449-9db2-4b2e-852f-28f745aa7e2a", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["311372"], "spl_set_id": ["6703e4f3-e9b8-4c70-9085-3d6ac0d7fbda"], "manufacturer_name": ["HEB"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (37808-529-01)", "package_ndc": "37808-529-01", "marketing_start_date": "20180201"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (37808-529-11)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "37808-529-11", "marketing_start_date": "20180201"}, {"sample": false, "description": "30 BLISTER PACK in 1 CARTON (37808-529-31)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "37808-529-31", "marketing_start_date": "20180201"}], "brand_name": "Loratadine Allergy Relief", "product_id": "37808-529_c624b449-9db2-4b2e-852f-28f745aa7e2a", "dosage_form": "TABLET", "product_ndc": "37808-529", "generic_name": "Loratadine", "labeler_name": "HEB", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loratadine Allergy Relief", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "ANDA076134", "marketing_category": "ANDA", "marketing_start_date": "20180201", "listing_expiration_date": "20261231"}