01 1ACELLA
02 2ACTAVIS ELIZABETH
03 3ALEMBIC
04 3ALKEM LABS LTD
05 3AUROBINDO PHARMA
06 3AUROBINDO PHARMA USA
07 2BAYER PHARMS
08 2CHASE LABS NJ
09 1ELITE PHARM SOLUTION
10 3ENDO OPERATIONS
11 2HERITAGE PHARMA
12 2MARTEC USA LLC
13 1NORVIUM BIOSCIENCE
14 3NORWICH
15 6NOVAST LABS
16 3OSMOTICA PHARM US
17 5PFIZER
18 6RISING
19 3SPIL
20 2SWISS PHARM
21 1TEVA
22 3TWI PHARMS
23 5VALEANT PHARMS NORTH
24 2VELZEN PHARMA PVT
25 1WATSON LABS
26 1WATSON LABS TEVA
27 6ZYDUS PHARMS
01 14CAPSULE;ORAL
02 1TABLET, EXTENDED RELEASE; ORAL
03 60TABLET, EXTENDED RELEASE;ORAL
01 28DISCN
02 46RX
03 1Blank
01 2ADALAT
02 3ADALAT CC
03 2AFEDITAB CR
04 63NIFEDIPINE
05 2PROCARDIA
06 3PROCARDIA XL
01 66No
02 8Yes
03 1Blank
RLD : Yes
TE Code :
Brand Name : ADALAT CC
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1993-04-21
Application Number : 20198
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : ADALAT CC
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 60MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1993-04-21
Application Number : 20198
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : ADALAT CC
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 90MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1993-04-21
Application Number : 20198
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Brand Name : ADALAT
Dosage Form : CAPSULE;ORAL
Dosage Strength : 10MG
Approval Date : 1985-11-27
Application Number : 19478
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : ADALAT
Dosage Form : CAPSULE;ORAL
Dosage Strength : 20MG
Approval Date : 1986-09-17
Application Number : 19478
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code : AB
Brand Name : PROCARDIA
Dosage Form : CAPSULE;ORAL
Dosage Strength : 10MG
Approval Date : 1982-01-01
Application Number : 18482
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code :
Brand Name : PROCARDIA
Dosage Form : CAPSULE;ORAL
Dosage Strength : 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1986-07-24
Application Number : 18482
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code : AB2
Brand Name : PROCARDIA XL
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 30MG
Approval Date : 1989-09-06
Application Number : 19684
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB2
RLD : Yes
TE Code : AB2
Brand Name : PROCARDIA XL
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 60MG
Approval Date : 1989-09-06
Application Number : 19684
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB2
RLD : Yes
TE Code : AB2
Brand Name : PROCARDIA XL
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 90MG
Approval Date : 1989-09-06
Application Number : 19684
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB2
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