folcyteine

Generic: multivitamin

Labeler: puretek corporation
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name folcyteine
Generic Name multivitamin
Labeler puretek corporation
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetylcysteine 200 mg/1, calcium citrate 47 mg/1, cholecalciferol 800 [iU]/1, folic acid 1000 ug/1, magnesium citrate 16 mg/1

Manufacturer
PureTek Corporation

Identifiers & Regulatory

Product NDC 59088-795
Product ID 59088-795_04cf0026-e299-ffd5-e063-6294a90aca1f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2023-09-14

Pharmacologic Class

Established (EPC)
antidote [epc] antidote for acetaminophen overdose [epc] mucolytic [epc] vitamin d [epc]
Mechanism of Action
reduction activity [moa]
Chemical Structure
vitamin d [cs]
Physiologic Effect
decreased respiratory secretion viscosity [pe] increased glutathione concentration [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59088795
Hyphenated Format 59088-795

Supplemental Identifiers

UPC
0359088795545
UNII
WYQ7N0BPYC MLM29U2X85 1C6V77QF41 935E97BOY8 RHO26O1T9V
NUI
N0000175429 N0000175961 N0000008867 N0000175960 N0000175776 N0000175547 M0022797 N0000175952

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 folcyteine (source: ndc)
Generic Name multivitamin (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
  • 47 mg/1
  • 800 [iU]/1
  • 1000 ug/1
  • 16 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (59088-795-54)
source: ndc

Packages (1)

Ingredients (5)

acetylcysteine (200 mg/1) calcium citrate (47 mg/1) cholecalciferol (800 [iU]/1) folic acid (1000 ug/1) magnesium citrate (16 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "04cf0026-e299-ffd5-e063-6294a90aca1f", "openfda": {"nui": ["N0000175429", "N0000175961", "N0000008867", "N0000175960", "N0000175776", "N0000175547", "M0022797", "N0000175952"], "upc": ["0359088795545"], "unii": ["WYQ7N0BPYC", "MLM29U2X85", "1C6V77QF41", "935E97BOY8", "RHO26O1T9V"], "spl_set_id": ["04cf0026-e29b-ffd5-e063-6294a90aca1f"], "pharm_class_cs": ["Vitamin D [CS]"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Glutathione Concentration [PE]"], "pharm_class_epc": ["Antidote [EPC]", "Antidote for Acetaminophen Overdose [EPC]", "Mucolytic [EPC]", "Vitamin D [EPC]"], "pharm_class_moa": ["Reduction Activity [MoA]"], "manufacturer_name": ["PureTek Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (59088-795-54)", "package_ndc": "59088-795-54", "marketing_start_date": "20230914"}], "brand_name": "Folcyteine", "product_id": "59088-795_04cf0026-e299-ffd5-e063-6294a90aca1f", "dosage_form": "TABLET", "pharm_class": ["Antidote [EPC]", "Antidote for Acetaminophen Overdose [EPC]", "Blood Coagulation Factor [EPC]", "Calcium [CS]", "Calculi Dissolution Agent [EPC]", "Cations", "Divalent [CS]", "Decreased Respiratory Secretion Viscosity [PE]", "Increased Coagulation Factor Activity [PE]", "Increased Glutathione Concentration [PE]", "Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]", "Magnesium Ion Exchange Activity [MoA]", "Mucolytic [EPC]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]", "Reduction Activity [MoA]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]", "Vitamin D [CS]", "Vitamin D [EPC]"], "product_ndc": "59088-795", "generic_name": "Multivitamin", "labeler_name": "PureTek Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Folcyteine", "active_ingredients": [{"name": "ACETYLCYSTEINE", "strength": "200 mg/1"}, {"name": "CALCIUM CITRATE", "strength": "47 mg/1"}, {"name": "CHOLECALCIFEROL", "strength": "800 [iU]/1"}, {"name": "FOLIC ACID", "strength": "1000 ug/1"}, {"name": "MAGNESIUM CITRATE", "strength": "16 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20230914", "listing_expiration_date": "20261231"}