01 2ABRAXIS PHARM
02 11ANI PHARMS
03 9APOTHECON
04 3ASCOT
05 2CAPLIN
06 2GLAND PHARMA LTD
07 1HIKMA
08 3HOSPIRA
09 4IDT AUSTRALIA LTD
10 2INTL MEDICATION
11 1INWOOD LABS
12 3IVAX SUB TEVA PHARMS
13 2KING PHARMS
14 2LANNETT
15 3LEDERLE
16 2NEXUS
17 1PANRAY
18 4PARKE DAVIS
19 3PARKEDALE
20 2PHARMAFAIR
21 2QUAD PHARMS
22 2ROXANE
23 1SANDOZ
24 2SMITH AND NEPHEW
25 1SOLOPAK
26 2VANGARD
27 2WARNER CHILCOTT
28 17WATSON LABS
29 1WEST-WARD PHARMS INT
01 35CAPSULE;ORAL
02 26INJECTABLE;INJECTION
03 2Injectable; Injection
04 26TABLET, EXTENDED RELEASE;ORAL
05 3TABLET;ORAL
01 77DISCN
02 9RX
03 6Blank
01 2PROCAINAMIDE HCL
02 71PROCAINAMIDE HYDROCHLORIDE
03 3PROCAN
04 4PROCAN SR
05 2PROCANBID
06 1PROCAPAN
07 8PRONESTYL
08 1PRONESTYL-SR
01 78No
02 8Yes
03 6Blank
RLD : Yes
TE Code :
Brand Name : PRONESTYL
Dosage Form : CAPSULE;ORAL
Dosage Strength : 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 7335
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : PRONESTYL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 100MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 7335
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : PRONESTYL
Dosage Form : CAPSULE;ORAL
Dosage Strength : 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 7335
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : PRONESTYL
Dosage Form : CAPSULE;ORAL
Dosage Strength : 375MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 7335
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : PRONESTYL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 500MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 7335
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Brand Name : PRONESTYL
Dosage Form : TABLET;ORAL
Dosage Strength : 250MG
Approval Date : 1982-01-01
Application Number : 17371
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : PRONESTYL
Dosage Form : TABLET;ORAL
Dosage Strength : 375MG
Approval Date : 1982-01-01
Application Number : 17371
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : PRONESTYL
Dosage Form : TABLET;ORAL
Dosage Strength : 500MG
Approval Date : 1982-01-01
Application Number : 17371
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : PROCANBID
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 500MG
Approval Date : 1996-01-31
Application Number : 20545
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : PROCANBID
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 1GM
Approval Date : 1996-01-31
Application Number : 20545
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
