Zolpidem
Ambien, Edluar (zolpidem) is a small molecule pharmaceutical. Zolpidem was first approved as Ambien on 1992-12-16. It is used to treat sleep initiation and maintenance disorders in the USA. The pharmaceutical is active against gamma-aminobutyric acid receptor subunit alpha-1. In addition, it is known to target gamma-aminobutyric acid receptor subunit alpha-3 and gamma-aminobutyric acid receptor subunit alpha-2.
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Commercial
Trade Name
FDA
EMA
Ambien, Edluar (generic drugs available since 2007-04-23, discontinued: Intermezzo, Tovalt, Zolpimist)
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Labels
FDA
EMA
Brand Name | Status | Last Update |
---|---|---|
ambien | New Drug Application | 2019-02-12 |
edluar | New Drug Application | 2019-08-15 |
zolpidem tartrate | ANDA | 2023-06-08 |
Agency Specific
FDA
EMA
No data
Patent Expiration
Patent | Expires | Flag | FDA Information |
---|---|---|---|
Zolpidem Tartrate, Zolpimist, Aytu | |||
8236285 | 2032-08-07 | DS, DP | U-70 |
Zolpidem Tartrate, Edluar, Mylan Speciality Lp | |||
9265720 | 2031-02-25 | U-674 | |
9597281 | 2027-04-06 | U-674 | |
Zolpidem Tartrate, Intermezzo, Purdue Pharma | |||
8242131 | 2029-08-20 | U-1266 | |
7658945 | 2027-04-15 | DP | U-1194 |
7682628 | 2025-02-16 | U-1194 | |
8252809 | 2025-02-16 | DP |
HCPCS
No data
Clinical
Clinical Trials
15 clinical trials
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Indications Phases 4
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Migraine disorders | D008881 | EFO_0003821 | G43 | 5 | — | 3 | 3 | 1 | 12 |
Cluster headache | D003027 | HP_0012199 | G44.00 | — | — | — | 1 | — | 1 |
Indications Phases 3
No data
Indications Phases 2
No data
Indications Without Phase
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Headache disorders | D020773 | EFO_0009550 | G44 | — | — | — | — | 1 | 1 |
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name | ZOLPIDEM |
INN | zolpidem |
Description | Zolpidem is an imidazo[1,2-a]pyridine compound having a 4-tolyl group at the 2-position, an N,N-dimethylcarbamoylmethyl group at the 3-position and a methyl substituent at the 6-position. It has a role as a central nervous system depressant, a GABA agonist and a sedative. |
Classification | Small molecule |
Drug class | hypnotics/sedatives (zolpidem type) |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | Cc1ccc(-c2nc3ccc(C)cn3c2CC(=O)N(C)C)cc1 |
Identifiers
PDB | — |
CAS-ID | 82626-48-0 |
RxCUI | 39993 |
ChEMBL ID | CHEMBL911 |
ChEBI ID | 10125 |
PubChem CID | 5732 |
DrugBank | DB00425 |
UNII ID | 7K383OQI23 (ChemIDplus, GSRS) |
Target
Agency Approved
GABRA1
GABRA1
Organism
Homo sapiens
Gene name
GABRA1
Gene synonyms
NCBI Gene ID
Protein name
gamma-aminobutyric acid receptor subunit alpha-1
Protein synonyms
GABA(A) receptor subunit alpha-1, GABA(A) receptor, alpha 1, gamma-aminobutyric acid (GABA) A receptor, alpha 1, gamma-aminobutyric acid type A receptor alpha1 subunit
Uniprot ID
Mouse ortholog
Gabra1 (14394)
gamma-aminobutyric acid receptor subunit alpha-1 (P62812)
Alternate
GABRA3
GABRA3
GABRA2
GABRA2
Organism
Homo sapiens
Gene name
GABRA3
Gene synonyms
NCBI Gene ID
Protein name
gamma-aminobutyric acid receptor subunit alpha-3
Protein synonyms
GABA(A) receptor subunit alpha-3, GABA(A) receptor, alpha 3, gamma-aminobutyric acid (GABA) A receptor, alpha 3, gamma-aminobutyric acid type A receptor alpha3 subunit, gamma-animobutyric acid (GABA) A receptor, alpha 3
Uniprot ID
Mouse ortholog
Gabra3 (14396)
gamma-aminobutyric acid receptor subunit alpha-3 (P26049)
Variants
Clinical Variant
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 8,048 documents
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Safety
Black-box Warning
Black-box warning for: Ambien , Edluar, Zolpidem tartrate
Adverse Events
Top Adverse Reactions
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2,763 adverse events reported
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