Drugs@FDA: FDA Approved Drug Products

Home | Previous Page

Abbreviated New Drug Application (ANDA): 075575
Company: WATSON LABS INC
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
AMMONIUM LACTATE AMMONIUM LACTATE EQ 12% BASE LOTION;TOPICAL Prescription AB No No
Original Approvals or Tentative Approvals
Action Date Submission Action Type Submission Classification Review Priority; Orphan Status Letters, Reviews, Labels, Patient Package Insert Notes Url
06/11/2002 ORIG-1 Approval

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
11/25/2008 SUPPL-9 Labeling

Label is not available on this site.

05/13/2003 SUPPL-2 Labeling

Label is not available on this site.

AMMONIUM LACTATE

LOTION;TOPICAL; EQ 12% BASE
TE Code = AB

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
AMMONIUM LACTATE AMMONIUM LACTATE EQ 12% BASE LOTION;TOPICAL Prescription No AB 075570 PERRIGO NEW YORK
AMMONIUM LACTATE AMMONIUM LACTATE EQ 12% BASE LOTION;TOPICAL Prescription No AB 076216 TARO
AMMONIUM LACTATE AMMONIUM LACTATE EQ 12% BASE LOTION;TOPICAL Prescription No AB 075575 WATSON LABS INC

Note: If you need help accessing information in different file formats, see Instructions for Downloading Viewers and Players.
Language Assistance Available: Español | 繁體中文 | Tiếng Việt | 한국어 | Tagalog | Русский | العربية | Kreyòl Ayisyen | Français | Polski | Português | Italiano | Deutsch | 日本語 | فارسی | English