loratadine

Generic: loratadine

Labeler: camber consumer care inc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name loratadine
Generic Name loratadine
Labeler camber consumer care inc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

loratadine 10 mg/1

Manufacturer
Camber Consumer Care Inc

Identifiers & Regulatory

Product NDC 69230-323
Product ID 69230-323_04d9c5a8-1f42-f7c0-e063-6294a90a92ae
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA211718
Listing Expiration 2026-12-31
Marketing Start 2023-07-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69230323
Hyphenated Format 69230-323

Supplemental Identifiers

RxCUI
311372
UPC
0369230323342 0369230323335 0369230323304
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 ANDA211718 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 10 BLISTER PACK in 1 CARTON (69230-323-01) / 10 TABLET in 1 BLISTER PACK (69230-323-32)
  • 1000 TABLET in 1 BOTTLE (69230-323-10)
  • 1 BOTTLE in 1 CARTON (69230-323-30) / 30 TABLET in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (69230-323-31) / 108 TABLET in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (69230-323-33) / 100 TABLET in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (69230-323-34) / 300 TABLET in 1 BOTTLE
source: ndc

Packages (6)

Ingredients (1)

loratadine (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "04d9c5a8-1f42-f7c0-e063-6294a90a92ae", "openfda": {"upc": ["0369230323342", "0369230323335", "0369230323304"], "unii": ["7AJO3BO7QN"], "rxcui": ["311372"], "spl_set_id": ["d57da4bd-af37-414a-a50c-e80d2bb28314"], "manufacturer_name": ["Camber Consumer Care Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 CARTON (69230-323-01)  / 10 TABLET in 1 BLISTER PACK (69230-323-32)", "package_ndc": "69230-323-01", "marketing_start_date": "20230728"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (69230-323-10)", "package_ndc": "69230-323-10", "marketing_start_date": "20230728"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (69230-323-30)  / 30 TABLET in 1 BOTTLE", "package_ndc": "69230-323-30", "marketing_start_date": "20230728"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (69230-323-31)  / 108 TABLET in 1 BOTTLE", "package_ndc": "69230-323-31", "marketing_start_date": "20230728"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (69230-323-33)  / 100 TABLET in 1 BOTTLE", "package_ndc": "69230-323-33", "marketing_start_date": "20230728"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (69230-323-34)  / 300 TABLET in 1 BOTTLE", "package_ndc": "69230-323-34", "marketing_start_date": "20230728"}], "brand_name": "Loratadine", "product_id": "69230-323_04d9c5a8-1f42-f7c0-e063-6294a90a92ae", "dosage_form": "TABLET", "product_ndc": "69230-323", "generic_name": "Loratadine", "labeler_name": "Camber Consumer Care Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loratadine", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "ANDA211718", "marketing_category": "ANDA", "marketing_start_date": "20230728", "listing_expiration_date": "20261231"}