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Nasal spray compositions exhibiting increased retention in the nasal cavity

Patent 5897858 Issued on April 27, 1999. Estimated Expiration Date: Icon_subject November 4, 2017. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

Patent References

Sustained release intranasal formulation and method of use thereof
Patent #: 4581225
Issued on: 04/08/1986
Inventor: Su ,   et al.

Fruity flavored nasal decongestant composition
Patent #: 5114979
Issued on: 05/19/1992
Inventor: Kielley

5116847

Inventors

Assignee

Application

No. 964038 filed on 11/04/1997

US Classes:

424/78.04, Ophthalmic preparation424/78.08, SOLID SYNTHETIC ORGANIC POLYMER AS DESIGNATED ORGANIC ACTIVE INGREDIENT (DOAI)424/434, Mucosal (e.g., nasal, etc.)424/601, Phosphorus or phosphorus compound514/772.5, Heterocyclic monomer514/853, DECONGESTANT514/912, OPHTHALMIC514/937DISPERSION OR EMULSION

Examiners

Primary: Bawa, Raj

Attorney, Agent or Firm

Foreign Patent References

  • 109561 EP. 05/12/1984
  • 0 380 367 EP. 08/12/1990
  • 0454617 EP. 10/12/1991
  • 0571671 EP. 12/12/1993
  • 94/05330 WO. 03/12/1994

International Class

A61K 009/08

Abstract

Aqueous nasal spray compositions containing:0.001-2% by weight/volume of a medicament selected from the group consisting of chlorpheniramine maleate, oxymetazoline hydrochloride and mixtures thereof;0.50 to 15.00% by weight/volume of a water soluble polymer selected from the group consisting of polyvinylpyrrolidone having an average molecular weight of about 10,000 to 360,000 and mixtures thereof;2.5 to 10.00% by weight/volume of polyethylene glycol;1.00 to 10.00% by weight/volume of a moisturizing agent other than polyethylene glycol;0.01 to 0.05% by weight/volume of disodium edetate;0.001 to 0.3% by weight/volume of an antimicrobial preservative;0.20 to 5.00% by weight/volume of an aromatic alcohol;a sufficient amount of a pharmaceutically acceptable buffer to maintain the pH of the composition within the range of about 4.0 to 8.0; andQS water.

Other References

  • Gennaro, A. R. (1985). Remington's Pharmaceutical Sciences, Mack Pub., Co., pp. 889 & 1500
  • Martindale--The Extra Pharmacopoeia (1989) p.841
  • Remington's Pharmaceutical Sciences (1985) pp. 889, 1127, 1159, 1299, 1305, 1309 and 1500, Mack Publishing Co
  • Chem Abs. vol. 116; No. 18; No. 181179, May 7, 1992, JP-A-04026617
  • Chem Abs vol. 108; No. 24, No. 210213, Jun. 13, 1988, JP-A-6222313
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