tricitrates

Generic: tricitrates

Labeler: chartwell rx, llc
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name tricitrates
Generic Name tricitrates
Labeler chartwell rx, llc
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

citric acid monohydrate 334 mg/5mL, potassium citrate 550 mg/5mL, sodium citrate 500 mg/5mL

Manufacturer
Chartwell RX, LLC

Identifiers & Regulatory

Product NDC 62135-438
Product ID 62135-438_33d7941b-0652-9528-e063-6394a90a8a55
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2022-12-08

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 62135438
Hyphenated Format 62135-438

Supplemental Identifiers

RxCUI
309317
UPC
0362135438470
UNII
2968PHW8QP EE90ONI6FF 1Q73Q2JULR

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 tricitrates (source: ndc)
Generic Name tricitrates (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 334 mg/5mL
  • 550 mg/5mL
  • 500 mg/5mL
source: ndc
Packaging
  • 2 TRAY in 1 BOX (62135-438-24) / 10 CUP in 1 TRAY / 5 mL in 1 CUP (62135-438-05)
  • 473 mL in 1 BOTTLE (62135-438-47)
source: ndc

Packages (2)

62135-438-24 2 TRAY in 1 BOX (62135-438-24) / 10 CUP in 1 TRAY / 5 mL in 1 CUP (62135-438-05) 62135-438-47 473 mL in 1 BOTTLE (62135-438-47)

Ingredients (3)

citric acid monohydrate (334 mg/5mL) potassium citrate (550 mg/5mL) sodium citrate (500 mg/5mL)

Linked Drug Pages (1)

Tricitrates ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "33d7941b-0652-9528-e063-6394a90a8a55", "openfda": {"upc": ["0362135438470"], "unii": ["2968PHW8QP", "EE90ONI6FF", "1Q73Q2JULR"], "rxcui": ["309317"], "spl_set_id": ["2a80ea6b-6334-4c33-a35e-a5cb2939fbcb"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 TRAY in 1 BOX (62135-438-24)  / 10 CUP in 1 TRAY / 5 mL in 1 CUP (62135-438-05)", "package_ndc": "62135-438-24", "marketing_start_date": "20250415"}, {"sample": false, "description": "473 mL in 1 BOTTLE (62135-438-47)", "package_ndc": "62135-438-47", "marketing_start_date": "20221208"}], "brand_name": "Tricitrates", "product_id": "62135-438_33d7941b-0652-9528-e063-6394a90a8a55", "dosage_form": "SOLUTION", "pharm_class": ["Acidifying Activity [MoA]", "Acidifying Activity [MoA]", "Acidifying Activity [MoA]", "Anti-coagulant [EPC]", "Anti-coagulant [EPC]", "Anti-coagulant [EPC]", "Calcium Chelating Activity [MoA]", "Calcium Chelating Activity [MoA]", "Calcium Chelating Activity [MoA]", "Calculi Dissolution Agent [EPC]", "Calculi Dissolution Agent [EPC]", "Calculi Dissolution Agent [EPC]", "Decreased Coagulation Factor Activity [PE]", "Decreased Coagulation Factor Activity [PE]", "Decreased Coagulation Factor Activity [PE]"], "product_ndc": "62135-438", "generic_name": "Tricitrates", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tricitrates", "active_ingredients": [{"name": "CITRIC ACID MONOHYDRATE", "strength": "334 mg/5mL"}, {"name": "POTASSIUM CITRATE", "strength": "550 mg/5mL"}, {"name": "SODIUM CITRATE", "strength": "500 mg/5mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20221208", "listing_expiration_date": "20261231"}