loratadine
Generic: loratadine
Labeler: camber consumer care incDrug Facts
Product Profile
Brand Name
loratadine
Generic Name
loratadine
Labeler
camber consumer care inc
Dosage Form
TABLET
Routes
Active Ingredients
loratadine 10 mg/1
Manufacturer
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
UPC
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 10 mg/1
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
Packages (6)
69230-323-01
10 BLISTER PACK in 1 CARTON (69230-323-01) / 10 TABLET in 1 BLISTER PACK (69230-323-32)
69230-323-10
1000 TABLET in 1 BOTTLE (69230-323-10)
69230-323-30
1 BOTTLE in 1 CARTON (69230-323-30) / 30 TABLET in 1 BOTTLE
69230-323-31
1 BOTTLE in 1 CARTON (69230-323-31) / 108 TABLET in 1 BOTTLE
69230-323-33
1 BOTTLE in 1 CARTON (69230-323-33) / 100 TABLET in 1 BOTTLE
69230-323-34
1 BOTTLE in 1 CARTON (69230-323-34) / 300 TABLET in 1 BOTTLE
Ingredients (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"}