Visitor Monitoring Drug History: IMIPRAMINE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: IMIPRAMINE HYDROCHLORIDE
FDA Application No: (ANDA) 083729
Active Ingredient(s): IMIPRAMINE HYDROCHLORIDE
Company: TEVA
 
Label History
 
Labels are not available on this site for IMIPRAMINE HYDROCHLORIDE, (ANDA) 083729
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
7/7/2000 357Facility Addition  
7/29/1997 356Chemistry  
6/18/1997 355Chemistry  
10/24/1996 354Chemistry  
10/10/1995 353Labeling  
2/8/1996 352Chemistry  
3/1/1995 350Chemistry  
9/19/1995 349Chemistry  
9/6/1994 348Chemistry  
6/17/1994 347Chemistry  
6/23/1993 346Labeling  
3/30/1992 345Chemistry  
4/12/1989 344Chemistry  
4/12/1989 343Chemistry  
4/12/1989 342Chemistry  
4/6/1989 341SBA  
3/31/1988 341Chemistry  
3/31/1988 340Chemistry  
11/4/1987 339Chemistry  
8/7/1987 338Chemistry  
9/10/1987 337Chemistry  
5/9/1986 336Chemistry  
3/12/1986 333Chemistry  
3/4/1986 331Chemistry  
2/5/1986 330Chemistry  
12/21/1984 328Chemistry  
2/5/1986 327Chemistry  
7/9/1984 326Chemistry  
2/3/1984 324Chemistry  
9/19/1983 323Chemistry  
3/17/1983 321Chemistry  
3/17/1983 320Chemistry  
12/16/1982 319Chemistry  
12/16/1982 317Chemistry  
6/25/1982 314Chemistry  
2/3/1984 313Chemistry  
2/3/1984 312Chemistry  
2/3/1984 311Chemistry  
6/25/1982 306Chemistry  
4/13/1982 303Chemistry  
6/27/1974 000Approval  
 
Therapeutic Equivalents
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