nauzene

Generic: sodium citrate

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

Drug Facts

Product Profile

Brand Name nauzene
Generic Name sodium citrate
Labeler kobayashi healthcare international, inc.
Dosage Form TABLET, CHEWABLE
Routes
ORAL
Active Ingredients

trisodium citrate dihydrate 230 mg/1

Manufacturer
Kobayashi Healthcare International, Inc.

Identifiers & Regulatory

Product NDC 52389-242
Product ID 52389-242_2d7c94e6-382b-1655-e063-6394a90a712d
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2000-07-08

Pharmacologic Class

Classes
acidifying activity [moa] anti-coagulant [epc] calcium chelating activity [moa] calculi dissolution agent [epc] decreased coagulation factor activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 52389242
Hyphenated Format 52389-242

Supplemental Identifiers

RxCUI
2002800
UPC
0072959420420
UNII
B22547B95K

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 nauzene (source: ndc)
Generic Name sodium citrate (source: ndc)
Application Number M001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 230 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (52389-242-10) / 10 TABLET, CHEWABLE in 1 BLISTER PACK
  • 3 BLISTER PACK in 1 CARTON (52389-242-42) / 14 TABLET, CHEWABLE in 1 BLISTER PACK
  • 4 BLISTER PACK in 1 CARTON (52389-242-56) / 14 TABLET, CHEWABLE in 1 BLISTER PACK
source: ndc

Packages (3)

52389-242-10 1 BLISTER PACK in 1 CARTON (52389-242-10) / 10 TABLET, CHEWABLE in 1 BLISTER PACK 52389-242-42 3 BLISTER PACK in 1 CARTON (52389-242-42) / 14 TABLET, CHEWABLE in 1 BLISTER PACK 52389-242-56 4 BLISTER PACK in 1 CARTON (52389-242-56) / 14 TABLET, CHEWABLE in 1 BLISTER PACK

Ingredients (1)

trisodium citrate dihydrate (230 mg/1)

Linked Drug Pages (1)

Nauzene ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2d7c94e6-382b-1655-e063-6394a90a712d", "openfda": {"upc": ["0072959420420"], "unii": ["B22547B95K"], "rxcui": ["2002800"], "spl_set_id": ["a60660b2-c5db-45a0-885f-de93e655380d"], "manufacturer_name": ["Kobayashi Healthcare International, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (52389-242-10)  / 10 TABLET, CHEWABLE in 1 BLISTER PACK", "package_ndc": "52389-242-10", "marketing_start_date": "20160715"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (52389-242-42)  / 14 TABLET, CHEWABLE in 1 BLISTER PACK", "package_ndc": "52389-242-42", "marketing_start_date": "20170706"}, {"sample": false, "description": "4 BLISTER PACK in 1 CARTON (52389-242-56)  / 14 TABLET, CHEWABLE in 1 BLISTER PACK", "package_ndc": "52389-242-56", "marketing_start_date": "20191116"}], "brand_name": "Nauzene", "product_id": "52389-242_2d7c94e6-382b-1655-e063-6394a90a712d", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Acidifying Activity [MoA]", "Anti-coagulant [EPC]", "Calcium Chelating Activity [MoA]", "Calculi Dissolution Agent [EPC]", "Decreased Coagulation Factor Activity [PE]"], "product_ndc": "52389-242", "generic_name": "Sodium Citrate", "labeler_name": "Kobayashi Healthcare International, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Nauzene", "active_ingredients": [{"name": "TRISODIUM CITRATE DIHYDRATE", "strength": "230 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20000708", "listing_expiration_date": "20261231"}