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Drug ReportsMicrocrystalline cellulose
Microcrystalline cellulose
Dibasic, Monobasic, Monohydrate, Phosphate (microcrystalline cellulose) is an unknown pharmaceutical. Microcrystalline cellulose was first approved as Sodium phosphates in plastic container on 1983-05-10.
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Drug Products
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New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
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Labels
FDA
EMA
Brand Name
Status
Last Update
liquidguardunapproved drug other2020-08-09
osmoprepNew Drug Application2010-06-04
potassium phosphatesNew Drug Application2025-04-15
sodium phosphatesANDA2025-08-08
Indications
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EMA
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Agency Specific
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EMA
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Patent Expiration
Patent
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FDA Information
Sodium Phosphate, Dibasic, Anhydrous / Sodium Phosphate, Monobasic, Monohydrate, Osmoprep, Salix Pharms
76870752028-06-22DS, DP
76870752028-06-22DS, DP
76870752028-06-22DS, DP
ATC Codes
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HCPCS
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Clinical
Clinical Trials
787 clinical trials
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Indications Phases 4
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Indications Phases 3
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Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
HypertriglyceridemiaD015228EFO_000421111
Indications Phases 1
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Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameMicrocrystalline cellulose
INN_
Description
DEAE-cellulose is a glycoside.
Classification
Unknown
Drug class
Image (chem structure or protein)Loading
Structure (InChI/SMILES or Protein Sequence)
Identifiers
PDB
CAS-ID618-482-1
RxCUI
ChEMBL IDCHEMBL4297557
ChEBI ID
PubChem CID
DrugBank
UNII IDX6JU3FX5UU (ChemIDplus, GSRS)
Target
No data
Variants
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 15,199 documents
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Safety
Black-box Warning
Black-box warning for: Osmoprep
Adverse Events
Top Adverse Reactions
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810 adverse events reported
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