Levemir is a brand name of insulin detemir, approved by the FDA in the following formulation(s):
LEVEMIR (insulin detemir recombinant - injectable; subcutaneous)
Manufacturer: NOVO NORDISK INC
Approval date: June 16, 2005
Strength(s): 100 UNITS/ML [RLD]
Has a generic version of Levemir been approved?
No. There is currently no therapeutically equivalent version of Levemir available.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Levemir. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.
See also: About generic drugs.
Related Patents
Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.
Acylated insulin
Patent 5,750,497
Issued: May 12, 1998
Inventor(s): Havelund; Svend & Halstr.o slashed.m; John & Jonassen; Ib & Andersen; Asser Sloth & Markussen; Jan
Assignee(s): Novo Nordisk A/S
The present invention relates to human insulin derivatives having a protracted profile of action in which the A21 and B3 amino acid residues are, independently, any amino acid residue which can be coded for by the genetic code except Lys, Arg and Cys; Phe.sup.B1 may be deleted; the B30 amino acid residue is (a) a non-codable, lipophilic amino acid having from 10 to 24 carbon atoms in which case an acyl group of a carboxylic acid with up to 5 carbon atoms is bound to the E-amino group of Lys.sup.B29 ; (b) any amino acid residue which can be coded by the genetic code except Lys, Arg and Cys, in which case a lipophilic substituent is bound to the E-amino group of Lys.sup.B29 ; or (c) deleted, in which case a lipophilic substituent is bound to the E-amino group of LyS.sup.B29 ; and any Zn.sup.2+ complexes thereof; provided that when the B30 amino acid residue is Thr or Ala, the A21 and B3 amino acid residues are both Asn and Phe.sup.B1 is present, then the insulin derivative is a Zn.sup.2 + complex.Patent expiration dates:
- May 16, 2019✓✓✓
- May 16, 2019
Insulin preparations containing NaCl
Patent 5,866,538
Issued: February 2, 1999
Inventor(s): Norup; Elsebeth & Langkj.ae butted.r; Liselotte & Havelund; Svend
Assignee(s): Novo Nordisk A/S
Insulin preparations of superior chemical stability, comprising human insulin or an analogue or derivative thereof, glycerol and/or mannitol, and 5 to 100 mM of a halogenide are disclosed.Patent expiration dates:
- June 20, 2017✓
- June 20, 2017
Acylated insulin
Patent 6,011,007
Issued: January 4, 2000
Inventor(s): Havelund; Svend & Halstrom; John & Jonassen; Ib & Andersen; Asser Sloth & Markussen; Jan
Assignee(s): Novo Nordisk A/S
The present invention relates to protracted human insulin derivatives in which the A21 and the B3 amino acid residues are, independently, any amino acid residue which can be coded for by the genetic code except Lys, Arg and Cys; Phe.sup.B1 may be deleted; the B30 amino acid residue is (a) a non-codable, lipophilic amino acid having from 10 to 24 carbon atoms, in which case an acyl group of a carboxylic acid with up to 5 carbon atoms is bound to the .epsilon.-amino group of Lys.sup.B29 ; or (b) the B30 amino acid residue is deleted or is any amino acid residue which can be coded for by the genetic code except Lys, Arg and Cys, in any of which cases the .epsilon.-amino group of Lys.sup.B29 has a lipophilic substituent; and any Zn.sup.2+ complexes thereof with the proviso that when B30 is Thr or Ala and A21 and B3 are both Asn, and Phe.sup.B1 is present, then the insulin derivative is always present as a Zn.sup.2+ complex.Patent expiration dates:
- February 2, 2014✓✓✓
- February 2, 2014
Acylated insulin
Patent 6,869,930
Issued: March 22, 2005
Inventor(s): Havelund; Svend & Halstrom; John & Jonassen; Ib & Andersen; Asser Sloth & Markussen; Jan
Assignee(s): Novo Nordisk A/S
The present invention relates to protracted human insulin derivatives in which the A21 and the B3 amino acid residues are, independently, any amino acid residue which can be coded for by the genetic code except Lys, Arg and Cys; PheB1 may be deleted; the B30 amino acid residue is (a) a non-codable, lipophilic amino acid having from 10 to 24 carbon atoms, in which case an acyl group of a carboxylic acid with up to 5 carbon atoms is bound to the ε-amino group of LysB29; or (b) the B30 amino acid residue is deleted or is any amino acid residue which can be coded for by the genetic code except Lys, Arg and Cys, in any of which cases the ε-amino group of LysB29 has a lipophilic substituent; and any Zn2+ complexes thereof with the proviso that when B30 is Thr or Ala and A21 and B3 are both Asn, and PheB1 is present, then the insulin derivative is always present as a Zn2+ complex.Patent expiration dates:
- February 2, 2014✓✓✓
- February 2, 2014
See also...
- Levemir Consumer Information (Drugs.com)
- Levemir Cartridges Consumer Information (Wolters Kluwer)
- Levemir Vials Consumer Information (Wolters Kluwer)
- Levemir Consumer Information (Cerner Multum)
- Levemir FlexPen Consumer Information (Cerner Multum)
- Levemir Advanced Consumer Information (Micromedex)
- Levemir AHFS DI Monographs (ASHP)
- Insulin Detemir Cartridges Consumer Information (Wolters Kluwer)
- Insulin Detemir Vials Consumer Information (Wolters Kluwer)
- Insulin detemir Consumer Information (Cerner Multum)
- Insulin detemir Subcutaneous Advanced Consumer Information (Micromedex)
- Insulin Detemir AHFS DI Monographs (ASHP)
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