Drugs@FDA: FDA-Approved Drugs

Home | Previous Page

New Drug Application (NDA): 016942
Company: WESTWOOD SQUIBB
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
HALOTEX HALOPROGIN 1% CREAM;TOPICAL Discontinued None 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
08/06/1971 ORIG-1 Approval Type 1 - New Molecular Entity PRIORITY

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
05/28/1986 SUPPL-17 Labeling

Label is not available on this site.

04/26/1996 SUPPL-14 Labeling

Label is not available on this site.

04/26/1996 SUPPL-13 Labeling

Label is not available on this site.

12/22/1977 SUPPL-11 Labeling

Label is not available on this site.

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