ibuprofen pm

Generic: ibuprofen and diphenhydramine citrate

Labeler: kroger company
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ibuprofen pm
Generic Name ibuprofen and diphenhydramine citrate
Labeler kroger company
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

diphenhydramine citrate 38 mg/1, ibuprofen 200 mg/1

Manufacturer
KROGER COMPANY

Identifiers & Regulatory

Product NDC 30142-278
Product ID 30142-278_cc3a78e5-52f9-424b-ab27-1c4ab644c735
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA216204
Listing Expiration 2026-12-31
Marketing Start 2024-05-07

Pharmacologic Class

Established (EPC)
nonsteroidal anti-inflammatory drug [epc]
Mechanism of Action
cyclooxygenase inhibitors [moa]
Chemical Structure
anti-inflammatory agents, non-steroidal [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 30142278
Hyphenated Format 30142-278

Supplemental Identifiers

RxCUI
895664
UPC
0041260022029
UNII
4OD433S209 WK2XYI10QM
NUI
N0000000160 M0001335 N0000175722

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 ibuprofen pm (source: ndc)
Generic Name ibuprofen and diphenhydramine citrate (source: ndc)
Application Number ANDA216204 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 38 mg/1
  • 200 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (30142-278-80) / 80 TABLET, COATED in 1 BOTTLE
source: ndc

Packages (1)

30142-278-80 1 BOTTLE in 1 CARTON (30142-278-80) / 80 TABLET, COATED in 1 BOTTLE

Ingredients (2)

diphenhydramine citrate (38 mg/1) ibuprofen (200 mg/1)

Linked Drug Pages (1)

Ibuprofen PM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "cc3a78e5-52f9-424b-ab27-1c4ab644c735", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0041260022029"], "unii": ["4OD433S209", "WK2XYI10QM"], "rxcui": ["895664"], "spl_set_id": ["15e649c4-d75f-e8c1-e063-6294a90a7747"], "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": ["KROGER COMPANY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (30142-278-80)  / 80 TABLET, COATED in 1 BOTTLE", "package_ndc": "30142-278-80", "marketing_start_date": "20240507"}], "brand_name": "Ibuprofen PM", "product_id": "30142-278_cc3a78e5-52f9-424b-ab27-1c4ab644c735", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "30142-278", "generic_name": "Ibuprofen and Diphenhydramine Citrate", "labeler_name": "KROGER COMPANY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen PM", "active_ingredients": [{"name": "DIPHENHYDRAMINE CITRATE", "strength": "38 mg/1"}, {"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA216204", "marketing_category": "ANDA", "marketing_start_date": "20240507", "listing_expiration_date": "20261231"}