loratadine
Generic: loratadine
Labeler: dr. reddy's laboratories inc.Drug Facts
Product Profile
Brand Name
loratadine
Generic Name
loratadine
Labeler
dr. reddy's laboratories inc.
Dosage Form
TABLET
Routes
Active Ingredients
loratadine 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
43598-756
Product ID
43598-756_33224371-b336-2c1e-63dd-7a8ce9d195ff
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA212795
Listing Expiration
2026-12-31
Marketing Start
2021-05-19
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
43598756
Hyphenated Format
43598-756
Supplemental Identifiers
RxCUI
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
ANDA212795 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 1 BLISTER PACK in 1 CARTON (43598-756-10) / 10 TABLET in 1 BLISTER PACK
- 3 BLISTER PACK in 1 CARTON (43598-756-30) / 10 TABLET in 1 BLISTER PACK
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "33224371-b336-2c1e-63dd-7a8ce9d195ff", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["672558"], "spl_set_id": ["9357186a-9452-e139-01d8-6b8c6f6a2c6b"], "manufacturer_name": ["Dr. Reddy's Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (43598-756-10) / 10 TABLET in 1 BLISTER PACK", "package_ndc": "43598-756-10", "marketing_start_date": "20230714"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (43598-756-30) / 10 TABLET in 1 BLISTER PACK", "package_ndc": "43598-756-30", "marketing_start_date": "20230714"}], "brand_name": "Loratadine", "product_id": "43598-756_33224371-b336-2c1e-63dd-7a8ce9d195ff", "dosage_form": "TABLET", "product_ndc": "43598-756", "generic_name": "Loratadine", "labeler_name": "Dr. Reddy's Laboratories Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loratadine", "active_ingredients": [{"name": "LORATADINE", "strength": "5 mg/1"}], "application_number": "ANDA212795", "marketing_category": "ANDA", "marketing_start_date": "20210519", "listing_expiration_date": "20261231"}