01 6ACETAMINOPHEN; HYDROCODONE BITARTRATE
02 3ESTRADIOL ACETATE
03 1ETHINYL ESTRADIOL; NORETHINDRONE
04 8ETHINYL ESTRADIOL; NORETHINDRONE ACETATE
05 2ETIDRONATE DISODIUM
06 3FLUOXETINE HYDROCHLORIDE
07 1MESALAMINE
08 6RISEDRONATE SODIUM
01 1CAPSULE;ORAL
02 1TABLET, CHEWABLE, TABLET;ORAL
03 2TABLET, DELAYED RELEASE;ORAL
04 24TABLET;ORAL
05 1TABLET;ORAL-21
06 1TABLET;ORAL-28
01 10.0025MG;0.5MG
02 10.005MG;1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
03 10.01MG,0.01MG,N/A;1MG,N/A,N/A
04 10.01MG,0.01MG;1MG,N/A
05 20.02MG,0.03MG,0.035MG;1MG,1MG,1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
06 10.02MG;1MG
07 10.02MG;1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
08 10.035MG;0.4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
09 10.45MG
10 10.9MG
11 11.8MG
12 1150MG
13 1200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
14 130MG
15 1325MG;10MG
16 1325MG;2.5MG
17 2325MG;5MG
18 1325MG;7.5MG
19 235MG
20 1400MG
21 1400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
22 1500MG;10MG
23 15MG
24 175MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
25 1EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
26 1EQ 15MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
27 1EQ 20MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
01 25DISCN
02 5RX
RLD : No
TE Code :
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET; ORAL
Proprietary Name : NORCO
Dosage Strength : 325MG;5MG
Approval Date : 1997-06-25
Application Number : 40099
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET; ORAL
Proprietary Name : NORCO
Dosage Strength : 325MG;10MG
Approval Date : 1997-02-14
Application Number : 40148
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET; ORAL
Proprietary Name : HYDROCODONE BITARTRATE A...
Dosage Strength : 500MG;10MG
Approval Date : 1997-02-14
Application Number : 40148
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET; ORAL
Proprietary Name : NORCO
Dosage Strength : 325MG;7.5MG
Approval Date : 2000-09-12
Application Number : 40148
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET; ORAL
Proprietary Name : NORCO
Dosage Strength : 325MG;2.5MG
Approval Date : 2014-07-07
Application Number : 40148
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET; ORAL
Proprietary Name : NORCO
Dosage Strength : 325MG;5MG
Approval Date : 2014-07-07
Application Number : 40148
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : FEMTRACE
Dosage Strength : 0.45MG
Approval Date : 2004-08-20
Application Number : 21633
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : FEMTRACE
Dosage Strength : 0.9MG
Approval Date : 2004-08-20
Application Number : 21633
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : FEMTRACE
Dosage Strength : 1.8MG
Approval Date : 2004-08-20
Application Number : 21633
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
ETHINYL ESTRADIOL; NORETHINDRONE
Dosage Form : TABLET; ORAL
Proprietary Name : FEMCON FE
Dosage Strength : 0.035MG;0.4MG **Federal ...
Approval Date : 2003-11-14
Application Number : 21490
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
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