01 1ASCOT
02 3BAUSCH
03 1BAYSHORE PHARMS LLC
04 2GALT PHARMS
05 1HIKMA
06 1LUPIN
07 1PAI HOLDINGS PHARM
08 2RISING
09 1SAGENT PHARMS
10 6SANDOZ
11 3STEVENS J
12 3WATSON LABS
01 6INJECTABLE;INJECTION
02 9TABLET, EXTENDED RELEASE;ORAL
03 10TABLET;ORAL
01 15DISCN
02 10RX
01 1INVAGESIC
02 1INVAGESIC FORTE
03 2NORFLEX
04 1NORGESIC
05 1NORGESIC FORTE
06 13ORPHENADRINE CITRATE
07 4ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE
08 1ORPHENGESIC
09 1ORPHENGESIC FORTE
01 21No
02 4Yes
RLD : Yes
TE Code :
Brand Name : NORFLEX
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 12157
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
ASPIRIN; CAFFEINE; ORPHENADRINE CITRATE
Brand Name : NORGESIC
Dosage Form : TABLET;ORAL
Dosage Strength : 385MG;30MG;25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-10-27
Application Number : 13416
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
ASPIRIN; CAFFEINE; ORPHENADRINE CITRATE
Brand Name : NORGESIC FORTE
Dosage Form : TABLET;ORAL
Dosage Strength : 770MG;60MG;50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-10-27
Application Number : 13416
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code : AP
Brand Name : ORPHENADRINE CITRATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 30MG/ML
Approval Date : 2003-03-04
Application Number : 40463
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
RLD : No
TE Code :
Brand Name : ORPHENADRINE CITRATE
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 100MG
Approval Date : 2000-06-23
Application Number : 40368
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code : AB
Brand Name : ORPHENADRINE CITRATE
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 100MG
Approval Date : 1998-06-19
Application Number : 40284
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : Yes
TE Code :
Brand Name : NORFLEX
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 30MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 13055
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code : AB
Brand Name : ORPHENADRINE CITRATE
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 100MG
Approval Date : 1999-01-29
Application Number : 40249
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AP
Brand Name : ORPHENADRINE CITRATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 30MG/ML
Approval Date : 2006-05-24
Application Number : 40484
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
RLD : No
TE Code : AB
Brand Name : ORPHENADRINE CITRATE
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 100MG
Approval Date : 2000-02-15
Application Number : 40327
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
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