loratadine and pseudoephedrine

Generic: loratadine and pseudoephedrine sulfate

Labeler: rite aid
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name loratadine and pseudoephedrine
Generic Name loratadine and pseudoephedrine sulfate
Labeler rite aid
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

loratadine 10 mg/1, pseudoephedrine sulfate 240 mg/1

Manufacturer
Rite Aid

Identifiers & Regulatory

Product NDC 11822-9990
Product ID 11822-9990_ccbdd53a-d690-4df0-ad4b-13806b44f1aa
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA076557
Listing Expiration 2026-12-31
Marketing Start 2004-11-17

Pharmacologic Class

Classes
adrenergic alpha-agonists [moa] alpha-adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 118229990
Hyphenated Format 11822-9990

Supplemental Identifiers

RxCUI
1117562
UPC
0011822331555
UNII
7AJO3BO7QN Y9DL7QPE6B

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 loratadine and pseudoephedrine (source: ndc)
Generic Name loratadine and pseudoephedrine sulfate (source: ndc)
Application Number ANDA076557 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
  • 240 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (11822-9990-0) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
  • 1 BLISTER PACK in 1 CARTON (11822-9990-5) / 15 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
source: ndc

Packages (2)

11822-9990-0 1 BLISTER PACK in 1 CARTON (11822-9990-0) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK 11822-9990-5 1 BLISTER PACK in 1 CARTON (11822-9990-5) / 15 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Ingredients (2)

loratadine (10 mg/1) pseudoephedrine sulfate (240 mg/1)

Linked Drug Pages (1)

Loratadine and Pseudoephedrine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ccbdd53a-d690-4df0-ad4b-13806b44f1aa", "openfda": {"upc": ["0011822331555"], "unii": ["7AJO3BO7QN", "Y9DL7QPE6B"], "rxcui": ["1117562"], "spl_set_id": ["bb0f7653-378f-40b1-8ead-77999fcbd87b"], "manufacturer_name": ["Rite Aid"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (11822-9990-0)  / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "11822-9990-0", "marketing_start_date": "20041117"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (11822-9990-5)  / 15 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "11822-9990-5", "marketing_start_date": "20041117"}], "brand_name": "Loratadine and Pseudoephedrine", "product_id": "11822-9990_ccbdd53a-d690-4df0-ad4b-13806b44f1aa", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "11822-9990", "generic_name": "LORATADINE and PSEUDOEPHEDRINE SULFATE", "labeler_name": "Rite Aid", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loratadine and Pseudoephedrine", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}, {"name": "PSEUDOEPHEDRINE SULFATE", "strength": "240 mg/1"}], "application_number": "ANDA076557", "marketing_category": "ANDA", "marketing_start_date": "20041117", "listing_expiration_date": "20261231"}