allergy relief d

Generic: cetirizine hydrochloride, pseudoephedrine hydrochloride

Labeler: h e b
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name allergy relief d
Generic Name cetirizine hydrochloride, pseudoephedrine hydrochloride
Labeler h e b
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

cetirizine hydrochloride 5 mg/1, pseudoephedrine hydrochloride 120 mg/1

Manufacturer
H E B

Identifiers & Regulatory

Product NDC 37808-651
Product ID 37808-651_c97e5860-b35b-4959-926c-d555b8622dfa
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA210719
Listing Expiration 2026-12-31
Marketing Start 2021-02-18

Pharmacologic Class

Classes
adrenergic alpha-agonists [moa] histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc] alpha-adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 37808651
Hyphenated Format 37808-651

Supplemental Identifiers

RxCUI
1014571
UNII
64O047KTOA 6V9V2RYJ8N

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 allergy relief d (source: ndc)
Generic Name cetirizine hydrochloride, pseudoephedrine hydrochloride (source: ndc)
Application Number ANDA210719 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
  • 120 mg/1
source: ndc
Packaging
  • 12 BLISTER PACK in 1 CARTON (37808-651-53) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
  • 24 BLISTER PACK in 1 CARTON (37808-651-62) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
source: ndc

Packages (2)

37808-651-53 12 BLISTER PACK in 1 CARTON (37808-651-53) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK 37808-651-62 24 BLISTER PACK in 1 CARTON (37808-651-62) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

Ingredients (2)

cetirizine hydrochloride (5 mg/1) pseudoephedrine hydrochloride (120 mg/1)

Linked Drug Pages (1)

allergy relief d ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c97e5860-b35b-4959-926c-d555b8622dfa", "openfda": {"unii": ["64O047KTOA", "6V9V2RYJ8N"], "rxcui": ["1014571"], "spl_set_id": ["b3ca8aae-04f2-4c00-9fb5-ce3ed7e6f1bb"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 BLISTER PACK in 1 CARTON (37808-651-53)  / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "37808-651-53", "marketing_start_date": "20210224"}, {"sample": false, "description": "24 BLISTER PACK in 1 CARTON (37808-651-62)  / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "37808-651-62", "marketing_start_date": "20210218"}], "brand_name": "allergy relief d", "product_id": "37808-651_c97e5860-b35b-4959-926c-d555b8622dfa", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "37808-651", "generic_name": "cetirizine hydrochloride, pseudoephedrine hydrochloride", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "allergy relief d", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "5 mg/1"}, {"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA210719", "marketing_category": "ANDA", "marketing_start_date": "20210218", "listing_expiration_date": "20261231"}