01 2ABRAXIS PHARM
02 11ANI PHARMS
03 9APOTHECON
04 3ASCOT
05 2GLAND PHARMA LTD
06 1HIKMA
07 3HOSPIRA
08 4IDT AUSTRALIA LTD
09 2INTL MEDICATION
10 1INWOOD LABS
11 3IVAX SUB TEVA PHARMS
12 2KING PHARMS
13 2LANNETT
14 3LEDERLE
15 2NEXUS
16 1PANRAY
17 4PARKE DAVIS
18 3PARKEDALE
19 2PHARMAFAIR
20 2QUAD PHARMS
21 2ROXANE
22 1SANDOZ
23 2SMITH AND NEPHEW
24 1SOLOPAK
25 2VANGARD
26 2WARNER CHILCOTT
27 17WATSON LABS
28 1WEST-WARD PHARMS INT
01 35CAPSULE;ORAL
02 24INJECTABLE;INJECTION
03 2Injectable; Injection
04 26TABLET, EXTENDED RELEASE;ORAL
05 3TABLET;ORAL
01 77DISCN
02 7RX
03 6Blank
01 2PROCAINAMIDE HCL
02 69PROCAINAMIDE HYDROCHLORIDE
03 3PROCAN
04 4PROCAN SR
05 2PROCANBID
06 1PROCAPAN
07 8PRONESTYL
08 1PRONESTYL-SR
01 76No
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Dosage Strength : 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 100MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 375MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 500MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
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