Package 0135-1329-01

Brand: FLONASE Nighttime Allergy Relief

Generic: triprolidine hcl
NDC Package

Package Facts

Identity

Package NDC 0135-1329-01
Digits Only 0135132901
Product NDC 0135-1329
Product ID 0135-1329_669165f1-6d53-4020-8f01-fbd9cb09c99b
Description

1 BLISTER PACK in 1 CARTON (0135-1329-01) / 36 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Discontinued 2026-02-28
Brand FLONASE Nighttime Allergy Relief
Generic triprolidine hcl
Sample Package No

Linked Drug Pages (1)

FLONASE Nighttime Allergy Relief ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "669165f1-6d53-4020-8f01-fbd9cb09c99b", "openfda": {"unii": ["YAN7R5L890"], "rxcui": ["1099694", "2623978"], "spl_set_id": ["070fb5a4-1848-41e8-90bf-57e682de1762"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (0135-1329-01)  / 36 TABLET in 1 BLISTER PACK", "package_ndc": "0135-1329-01", "marketing_end_date": "20260228", "marketing_start_date": "20221215"}], "brand_name": "FLONASE Nighttime Allergy Relief", "product_id": "0135-1329_669165f1-6d53-4020-8f01-fbd9cb09c99b", "dosage_form": "TABLET", "product_ndc": "0135-1329", "generic_name": "triprolidine hcl", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "FLONASE", "brand_name_suffix": "Nighttime Allergy Relief", "active_ingredients": [{"name": "TRIPROLIDINE HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20260228", "marketing_start_date": "20221215"}