emetrol powder non-drowsy

Generic: sodium citrate dihydrate

Labeler: wellspring pharmaceutical corporation
NDC Directory HUMAN OTC DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name emetrol powder non-drowsy
Generic Name sodium citrate dihydrate
Labeler wellspring pharmaceutical corporation
Dosage Form POWDER, FOR SOLUTION
Routes
ORAL
Active Ingredients

trisodium citrate dihydrate 460 mg/1

Manufacturer
WellSpring Pharmaceutical Corporation

Identifiers & Regulatory

Product NDC 65197-203
Product ID 65197-203_a6121b17-e850-4677-9ad1-ceb36de16336
Product Type HUMAN OTC DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2023-12-01

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 65197203
Hyphenated Format 65197-203

Supplemental Identifiers

RxCUI
2671573 2671579
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 emetrol powder non-drowsy (source: ndc)
Generic Name sodium citrate dihydrate (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 460 mg/1
source: ndc
Packaging
  • 6 POWDER, FOR SOLUTION in 1 CARTON (65197-203-09)
source: ndc

Packages (1)

65197-203-09 6 POWDER, FOR SOLUTION in 1 CARTON (65197-203-09)

Ingredients (1)

trisodium citrate dihydrate (460 mg/1)

Linked Drug Pages (1)

Emetrol Powder Non-Drowsy ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a6121b17-e850-4677-9ad1-ceb36de16336", "openfda": {"unii": ["B22547B95K"], "rxcui": ["2671573", "2671579"], "spl_set_id": ["9d8d2ee7-9db7-4be7-8c73-511eb2e32459"], "manufacturer_name": ["WellSpring Pharmaceutical Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 POWDER, FOR SOLUTION in 1 CARTON (65197-203-09)", "package_ndc": "65197-203-09", "marketing_start_date": "20231201"}], "brand_name": "Emetrol Powder Non-Drowsy", "product_id": "65197-203_a6121b17-e850-4677-9ad1-ceb36de16336", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Acidifying Activity [MoA]", "Anti-coagulant [EPC]", "Calcium Chelating Activity [MoA]", "Calculi Dissolution Agent [EPC]", "Decreased Coagulation Factor Activity [PE]"], "product_ndc": "65197-203", "generic_name": "Sodium Citrate Dihydrate", "labeler_name": "WellSpring Pharmaceutical Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Emetrol Powder", "brand_name_suffix": "Non-Drowsy", "active_ingredients": [{"name": "TRISODIUM CITRATE DIHYDRATE", "strength": "460 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20231201", "listing_expiration_date": "20261231"}