loratadine

Generic: loratadine

Labeler: american health packaging
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name loratadine
Generic Name loratadine
Labeler american health packaging
Dosage Form TABLET
Routes
ORAL
Active Ingredients

loratadine 10 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 68084-248
Product ID 68084-248_276fa85f-4a61-3308-e063-6294a90aeda4
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA076134
Listing Expiration 2026-12-31
Marketing Start 2007-11-21

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68084248
Hyphenated Format 68084-248

Supplemental Identifiers

RxCUI
311372
UNII
7AJO3BO7QN

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
  • 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-248-01) / 1 TABLET in 1 BLISTER PACK (68084-248-11)
source: ndc

Packages (1)

68084-248-01 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-248-01) / 1 TABLET in 1 BLISTER PACK (68084-248-11)

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": "276fa85f-4a61-3308-e063-6294a90aeda4", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["311372"], "spl_set_id": ["411f3692-99ff-49d7-8594-e6f404f5861f"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-248-01)  / 1 TABLET in 1 BLISTER PACK (68084-248-11)", "package_ndc": "68084-248-01", "marketing_start_date": "20071121"}], "brand_name": "Loratadine", "product_id": "68084-248_276fa85f-4a61-3308-e063-6294a90aeda4", "dosage_form": "TABLET", "product_ndc": "68084-248", "generic_name": "Loratadine", "labeler_name": "American Health Packaging", "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": "20071121", "listing_expiration_date": "20261231"}