ibuprofen and pseudoephedrine hydrochloride
Generic: ibuprofen and pseudoephedrine hydrochloride
Labeler: the kroger companyDrug Facts
Product Profile
Brand Name
ibuprofen and pseudoephedrine hydrochloride
Generic Name
ibuprofen and pseudoephedrine hydrochloride
Labeler
the kroger company
Dosage Form
TABLET, SUGAR COATED
Routes
Active Ingredients
ibuprofen 200 mg/1, pseudoephedrine hydrochloride 30 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
30142-423
Product ID
30142-423_2a40a064-9ee8-9b1a-e063-6294a90a46ac
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA074567
Listing Expiration
2026-12-31
Marketing Start
2001-10-13
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
30142423
Hyphenated Format
30142-423
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
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
ibuprofen and pseudoephedrine hydrochloride (source: ndc)
Generic Name
ibuprofen and pseudoephedrine hydrochloride (source: ndc)
Application Number
ANDA074567 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/1
- 30 mg/1
Packaging
- 1 BLISTER PACK in 1 CARTON (30142-423-41) / 40 TABLET, SUGAR COATED in 1 BLISTER PACK
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a40a064-9ee8-9b1a-e063-6294a90a46ac", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0011110353658"], "unii": ["WK2XYI10QM", "6V9V2RYJ8N"], "rxcui": ["1299021"], "spl_set_id": ["2c15339d-a33b-4884-87d8-a3b50903a2c8"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["The Kroger Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (30142-423-41) / 40 TABLET, SUGAR COATED in 1 BLISTER PACK", "package_ndc": "30142-423-41", "marketing_start_date": "20011013"}], "brand_name": "Ibuprofen and Pseudoephedrine Hydrochloride", "product_id": "30142-423_2a40a064-9ee8-9b1a-e063-6294a90a46ac", "dosage_form": "TABLET, SUGAR COATED", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "30142-423", "generic_name": "Ibuprofen and Pseudoephedrine Hydrochloride", "labeler_name": "The Kroger Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen and Pseudoephedrine Hydrochloride", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}, {"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA074567", "marketing_category": "ANDA", "marketing_start_date": "20011013", "listing_expiration_date": "20261231"}