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01 1ABBVIE
02 2STRIDES PHARMA
03 1ABHAI LLC
04 3ACCORD HLTHCARE
05 1AIPING PHARM INC
06 3AJANTA PHARMA LTD
07 3AMNEAL PHARMS
08 1AVET LIFESCIENCES
09 1BEXIMCO PHARMS USA
10 3BIONPHARMA
11 2CHARTWELL RX
12 1HIBROW HLTHCARE
13 3IMPAX PHARMS
14 4JANSSEN PHARMS
15 2LANNETT CO INC
16 1LEADING
17 1MYLAN PHARMS INC
18 1NOVAST LABS
19 1NOVITIUM PHARMA
20 1ORTHO MCNEIL JANSSEN
21 3OSMOTICA PHARM US
22 2PHARM ASSOC
23 3PHARMOBEDIENT
24 1PHARMOBEDIENT CNSLTG
25 1QUANTUM PHARMICS
26 2RISING
27 3RUBICON RESEARCH
28 1TEVA PHARMS USA
29 1TRUPHARMA
30 3UNIQUE
31 1USL PHARMA
32 1WATSON LABS
33 3ZYDUS PHARMS
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01 2GEL;TRANSDERMAL
02 7SYRUP;ORAL
03 1TABLET, EXTENDED RELEASE; ORAL
04 33TABLET, EXTENDED RELEASE;ORAL
05 18TABLET;ORAL
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01 22DISCN
02 38RX
03 1Blank
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01 2DITROPAN
02 3DITROPAN XL
03 1GELNIQUE
04 54OXYBUTYNIN CHLORIDE
05 1Oxybutynin Chloride
01 54No
02 6Yes
03 1Blank
RLD : Yes
TE Code :
Brand Name : GELNIQUE
Dosage Form : GEL;TRANSDERMAL
Dosage Strength : 10% (100MG/PACKET) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 2009-01-27
Application Number : 22204
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code : AB
Brand Name : OXYBUTYNIN CHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Approval Date : 1997-10-31
Application Number : 75079
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : OXYBUTYNIN CHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Approval Date : 2020-12-17
Application Number : 208165
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : Yes
TE Code :
Brand Name : DITROPAN
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 17577
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : DITROPAN XL
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1998-12-16
Application Number : 20897
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : DITROPAN XL
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1998-12-16
Application Number : 20897
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : DITROPAN XL
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1999-06-22
Application Number : 20897
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : DITROPAN
Dosage Form : SYRUP;ORAL
Dosage Strength : 5MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 18211
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code : AB
Brand Name : OXYBUTYNIN CHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Approval Date : 1988-11-14
Application Number : 71655
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code :
Brand Name : OXYBUTYNIN CHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Approval Date : 1988-03-10
Application Number : 70746
RX/OTC/DISCN : DISCN
RLD : No
TE Code :