diurex ultimate

Generic: caffeine

Labeler: kobayashi healthcare international, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name diurex ultimate
Generic Name caffeine
Labeler kobayashi healthcare international, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

caffeine 100 mg/1

Manufacturer
Kobayashi Healthcare International, Inc.

Identifiers & Regulatory

Product NDC 52389-656
Product ID 52389-656_32bf9d60-d270-5848-e063-6294a90a8dcb
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M027
Listing Expiration 2026-12-31
Marketing Start 2015-10-31

Pharmacologic Class

Established (EPC)
central nervous system stimulant [epc] methylxanthine [epc]
Chemical Structure
xanthines [cs]
Physiologic Effect
central nervous system stimulation [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 52389656
Hyphenated Format 52389-656

Supplemental Identifiers

RxCUI
308853
UPC
0072959010560
UNII
3G6A5W338E
NUI
N0000175739 N0000175729 N0000175790 M0023046

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 diurex ultimate (source: ndc)
Generic Name caffeine (source: ndc)
Application Number M027 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 2 BLISTER PACK in 1 CARTON (52389-656-60) / 30 TABLET, FILM COATED in 1 BLISTER PACK (52389-656-01)
source: ndc

Packages (1)

52389-656-60 2 BLISTER PACK in 1 CARTON (52389-656-60) / 30 TABLET, FILM COATED in 1 BLISTER PACK (52389-656-01)

Ingredients (1)

caffeine (100 mg/1)

Linked Drug Pages (1)

Diurex Ultimate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "32bf9d60-d270-5848-e063-6294a90a8dcb", "openfda": {"nui": ["N0000175739", "N0000175729", "N0000175790", "M0023046"], "upc": ["0072959010560"], "unii": ["3G6A5W338E"], "rxcui": ["308853"], "spl_set_id": ["c6debbfe-6061-463f-8f17-fb240c6f1bab"], "pharm_class_cs": ["Xanthines [CS]"], "pharm_class_pe": ["Central Nervous System Stimulation [PE]"], "pharm_class_epc": ["Central Nervous System Stimulant [EPC]", "Methylxanthine [EPC]"], "manufacturer_name": ["Kobayashi Healthcare International, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (52389-656-60)  / 30 TABLET, FILM COATED in 1 BLISTER PACK (52389-656-01)", "package_ndc": "52389-656-60", "marketing_start_date": "20151031"}], "brand_name": "Diurex Ultimate", "product_id": "52389-656_32bf9d60-d270-5848-e063-6294a90a8dcb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]", "Methylxanthine [EPC]", "Xanthines [CS]"], "product_ndc": "52389-656", "generic_name": "Caffeine", "labeler_name": "Kobayashi Healthcare International, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Diurex", "brand_name_suffix": "Ultimate", "active_ingredients": [{"name": "CAFFEINE", "strength": "100 mg/1"}], "application_number": "M027", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20151031", "listing_expiration_date": "20261231"}