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Sinecatechins
Veregen (sinecatechins) is an unknown pharmaceutical. Sinecatechins was first approved as Veregen on 2006-10-31.
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Commercial
Therapeutic Areas
No data
Trade Name
FDA
EMA
Veregen
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Sinecatechins
Tradename
Company
Number
Date
Products
VEREGENANI PHARMSN-021902 RX2006-10-31
1 products, RLD, RS
Labels
FDA
EMA
Brand Name
Status
Last Update
veregenNew Drug Application2022-11-10
Indications
FDA
EMA
No data
Agency Specific
FDA
EMA
No data
Patent Expiration
Patent
Expires
Flag
FDA Information
Sinecatechins, Veregen, Ani Pharms
78586622026-10-02DPU-172
97704062025-07-12DPU-172
ATC Codes
D: Dermatologicals
— D06: Antibiotics and chemotherapeutics for dermatological use
— D06B: Chemotherapeutics for topical use
— D06BB: Antivirals, topical
— D06BB12: Sinecatechins
HCPCS
No data
Clinical
Clinical Trials
500 clinical trials
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Mock data
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
AnesthesiaD0007583510192964
General anesthesiaD00076812581227
Postoperative painD010149G89.1811161221
Emergence deliriumD000071257———6915
DeliriumD003693R41.011—6614
Postoperative cognitive complicationsD00007969021—2610
Breast neoplasmsD001943EFO_0003869C50—1—359
Postoperative nausea and vomitingD020250EFO_0004888———437
Respiratory distress syndromeD012128EFO_1000637J80——4217
HypotensionD007022EFO_0005251I95———336
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Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Postoperative complicationsD011183——1—34
AnalgesiaD000698——2—13
Respiratory insufficiencyD012131HP_0002093J96.9——2—13
Non-small-cell lung carcinomaD002289——1—12
Kidney transplantationD016030—11——2
Drug-related side effects and adverse reactionsD064420T88.71—1——2
Intratracheal intubationD007442——1—12
Aortic valve insufficiencyD001022EFO_00071481—1——2
Mitral valve insufficiencyD008944HP_00016531—1——2
Esophageal neoplasmsD004938C15——1——1
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Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Inguinal herniaD006552HP_0000023K40—1——23
Opioid-related disordersD009293EFO_0005611F11—1——23
Substance-related disordersD019966EFO_0003890F13—1——23
PhimosisD010688EFO_1001104N47.111———2
ParaphimosisD010263EFO_1001086N47.211———2
BalanitisD001446EFO_1000833N48.111———2
CryptorchidismD003456EFO_0004562Q53.1—1——12
Lung injuryD055370S27.3011——12
Atrial fibrillationD001281EFO_0000275I48.011——12
Radical mastectomyD01540911———1
Show 9 more
Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
InflammationD0072492———13
Chronic kidney failureD007676EFO_0003884N18.61————1
Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Inhalation anesthesiaD000769————44
Urinary bladder neoplasmsD001749C67————33
Myocardial ischemiaD017202EFO_1001375I20-I25————33
Cerebral palsyD002547G80————22
Operative surgical proceduresD013514————22
Mitochondrial diseasesD028361EFO_0000591————22
HemiarthroplastyD062785————22
Biliary atresiaD001656EFO_0004217Q44.2————22
RhytidoplastyD015361————11
Alzheimer diseaseD000544EFO_0000249F03————11
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Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameSINECATECHINS
INN—
Description
Sinecatechins (USAN, trade names Veregen and Polyphenon E) is a specific water extract of green tea leaves from Camellia sinensis that is the active ingredient in an ointment approved by the FDA in 2006 as a botanical drug to treat genital warts. Sinecatechins are mostly catechins, 55% of which is epigallocatechin gallate. It was the first botanical drug approved by the US FDA.
Classification
Unknown
Drug class—
Image (chem structure or protein)
Structure (InChI/SMILES or Protein Sequence)—
Identifiers
PDB—
CAS-ID—
RxCUI—
ChEMBL IDCHEMBL1201723
ChEBI ID—
PubChem CID—
DrugBank—
UNII ID—
Target
Agency Approved
No data
Alternate
No data
Variants
Clinical Variant
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
Mock data
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Additional graphs summarizing 230 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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5,428 adverse events reported
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