IP Library Patent Application 14748617
Patent Application
App. No. 14/748,617

PHARMACEUTICAL COMPOSITIONS

Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US None
App. No.
14/748,617
Abstract

Pharmaceutical compositions are provided which comprise effective amounts of analgesic to treat a subject, including to reduce or eliminate an adverse effect associated with the analgesic.

Claims (31)

1 - 22 . (canceled)

23 . A method for treating pain, the method comprising administering a solid oral dosage form to a subject in need thereof, wherein the solid oral dosage form comprises an immediate-release layer and a controlled-release layer, wherein the immediate-release layer comprises about 0.5-60 mg of promethazine or a pharmaceutical acceptable salt thereof and the controlled-release layer comprises an opioid analgesic and a non-opioid analgesic.

24 . The method of claim 23 , wherein the promethazine or a pharmaceutically acceptable salt thereof is present in an amount of about 12.5 mg.

25 . The method of claim 23 , wherein promethazine is present in an amount of about 11 mg.

26 . The method of claim 23 24 , wherein the pharmaceutically acceptable salt of the promethazine is promethazine hydrochloride and is present in an amount of about 12.5 mg.

27 . The method of claim 23 , wherein a pharmaceutically acceptable salt of the promethazine is promethazine hydrochloride.

28 . The method of claim 23 , wherein the opioid analgesic is hydrocodone, oxycodone, or a pharmaceutically acceptable salt thereof.

29 . The method of claim 28 , wherein the opioid analgesic is hydrocodone bitartrate.

30 . The method of claim 23 , wherein the non-opioid analgesic is acetaminophen or a pharmaceutically acceptable salt thereof.

31 . The method of claim 23 , wherein the solid oral dosage form is a bi-layer tablet.

32 . The method of claim 23 , wherein the pain is severe pain.

33 . A method for treating pain, the method comprising administering a solid oral dosage form to a subject in need thereof, wherein the solid oral dosage form comprises an immediate-release layer and a controlled-release layer, wherein the immediate-release layer comprises an antiemetic, and the controlled-release layer comprises a non-opioid analgesic and about 1-20 mg of hydrocodone, oxycodone, or a pharmaceutically acceptable salt thereof.

34 . The method of claim 33 , wherein the hydrocodone, oxycodone, or a pharmaceutically acceptable salt thereof is present in an amount of about 1 mg to about 15 mg.

35 . The method of claim 34 , wherein the hydrocodone or a pharmaceutically acceptable salt thereof is present in an amount of about 7.5 mg.

36 . The method of claim 34 , wherein the hydrocodone is present in an amount of about 5 mg.

37 . The method of claim 35 , wherein the pharmaceutically acceptable salt of the hydrocodone is hydrocodone bitartrate and is present in an amount of about 7.5 mg.

38 . The method of claim 34 , wherein the oxycodone or a pharmaceutically acceptable salt thereof is present in an amount of about 7.5 mg.

39 . The method of claim 33 , wherein a pharmaceutically acceptable salt of the hydrocodone is hydrocodone bitartrate.

40 . The method of claim 33 , wherein the antiemetic is promethazine or a pharmaceutically acceptable salt thereof.

41 . The method of claim 40 , wherein the antiemetic is promethazine hydrochloride.

42 . The method of claim 33 , wherein the non-opioid analgesic is acetaminophen or a pharmaceutically acceptable salt thereof.

43 . The method of claim 33 , wherein the solid oral dosage form is a bi-layer tablet.

44 . The method of claim 33 , wherein the pain is severe pain.

45 . A method for treating pain, the method comprising administering a solid oral dosage form to a subject in need thereof, wherein the solid oral dosage form comprises an immediate-release layer and a controlled-release layer, wherein the immediate-release layer comprises an antiemetic and the controlled-release layer comprises an opioid analgesic and about 200-600 mg of acetaminophen or a pharmaceutically acceptable salt thereof and an opioid analgesic.

46 . The method of claim 45 , wherein the acetaminophen or a pharmaceutically acceptable salt thereof is present in an amount of about 325 mg.

47 . The method of claim 45 , wherein the opioid analgesic is hydrocodone, oxycodone, or a pharmaceutically acceptable salt thereof.

48 . The method of claim 47 , wherein the opioid analgesic is hydrocodone bitartrate.

49 . The method of claim 45 , wherein the antiemetic is promethazine or a pharmaceutically acceptable salt thereof.

50 . The method of claim 49 , wherein the antiemetic is promethazine hydrochloride.

51 . The method of claim 45 , wherein the solid oral dosage form is a bi-layer tablet.

52 . The method of claim 45 , wherein the pain is severe pain.

Assignments (3)
CHANGE OF ADDRESS Recorded Dec 9, 2015
From: LOCL PHARMA, INC.
To: LOCL PHARMA, INC.
Reel/Frame 037255/0606 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 24, 2015
From: BOSSE, PAUL
To: CHARLESTON LABORATORIES, INC.
Reel/Frame 035895/0546 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 24, 2015
From: CHARLESTON LABORATORIES, INC.
To: LOCL PHARMA, INC.
Reel/Frame 035895/0560 →