exchange select all day allergy

Generic: cetirizine hydrochloride

Labeler: army & air force exchange service
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name exchange select all day allergy
Generic Name cetirizine hydrochloride
Labeler army & air force exchange service
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

cetirizine hydrochloride 10 mg/1

Manufacturer
Army & Air Force Exchange Service

Identifiers & Regulatory

Product NDC 55301-076
Product ID 55301-076_e61a6e00-ceae-4a3b-bbf8-ead4edc14d59
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA078336
Listing Expiration 2027-12-31
Marketing Start 2016-05-13

Pharmacologic Class

Classes
histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55301076
Hyphenated Format 55301-076

Supplemental Identifiers

RxCUI
1014678
UNII
64O047KTOA

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 exchange select all day allergy (source: ndc)
Generic Name cetirizine hydrochloride (source: ndc)
Application Number ANDA078336 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (55301-076-39) / 30 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (55301-076-95) / 45 TABLET, FILM COATED in 1 BOTTLE
source: ndc

Packages (2)

55301-076-39 1 BOTTLE in 1 CARTON (55301-076-39) / 30 TABLET, FILM COATED in 1 BOTTLE 55301-076-95 1 BOTTLE in 1 CARTON (55301-076-95) / 45 TABLET, FILM COATED in 1 BOTTLE

Ingredients (1)

cetirizine hydrochloride (10 mg/1)

Linked Drug Pages (1)

Exchange select all day allergy ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e61a6e00-ceae-4a3b-bbf8-ead4edc14d59", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["e7220494-3640-4b33-b577-ed3ca7c483e8"], "manufacturer_name": ["Army & Air Force Exchange Service"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (55301-076-39)  / 30 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "55301-076-39", "marketing_start_date": "20170829"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (55301-076-95)  / 45 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "55301-076-95", "marketing_start_date": "20160513"}], "brand_name": "Exchange select all day allergy", "product_id": "55301-076_e61a6e00-ceae-4a3b-bbf8-ead4edc14d59", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "55301-076", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Army & Air Force Exchange Service", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Exchange select all day allergy", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078336", "marketing_category": "ANDA", "marketing_start_date": "20160513", "listing_expiration_date": "20271231"}