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01 3ACETAMINOPHEN; HYDROCODONE BITARTRATE
02 2AMANTADINE HYDROCHLORIDE
03 5AMIODARONE HYDROCHLORIDE
04 1ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE
05 4BETHANECHOL CHLORIDE
06 1BEXAROTENE
07 1BRIMONIDINE TARTRATE
08 1BRIMONIDINE TARTRATE; TIMOLOL MALEATE
09 1BROMPHENIRAMINE MALEATE
10 3BUMETANIDE
11 1CALCITONIN SALMON RECOMBINANT
12 3CHLORDIAZEPOXIDE HYDROCHLORIDE
13 5CHLORPROMAZINE HYDROCHLORIDE
14 4CHOLESTYRAMINE
15 4CIMETIDINE
16 3CLOBAZAM
17 4DEFLAZACORT
18 2DEXAMETHASONE
19 1DIFLUPREDNATE
20 3DIVALPROEX SODIUM
21 3DROXIDOPA
22 1ELIGLUSTAT TARTRATE
23 1ETHACRYNIC ACID
24 1EXEMESTANE
25 1FLUOXETINE HYDROCHLORIDE
26 1FLUOXYMESTERONE
27 4FLUPHENAZINE HYDROCHLORIDE
28 6FLUVOXAMINE MALEATE
29 3FOSINOPRIL SODIUM
30 1GLUTETHIMIDE
31 4HYDRALAZINE HYDROCHLORIDE
32 1HYDROCHLOROTHIAZIDE; SPIRONOLACTONE
33 8ISOTRETINOIN
34 1MEDROXYPROGESTERONE ACETATE
35 2MEMANTINE HYDROCHLORIDE
36 2METHOCARBAMOL
37 3MIRTAZAPINE
38 9MORPHINE SULFATE
39 1MOXIFLOXACIN HYDROCHLORIDE
40 1NYSTATIN
41 2OXANDROLONE
42 1OXYBUTYNIN CHLORIDE
43 4PAROXETINE HYDROCHLORIDE
44 1PENTOXIFYLLINE
45 1PHENDIMETRAZINE TARTRATE
46 2PHENTERMINE HYDROCHLORIDE
47 8POTASSIUM CHLORIDE
48 2PREDNISONE
49 3PROPAFENONE HYDROCHLORIDE
50 4PROPRANOLOL HYDROCHLORIDE
51 1SODIUM POLYSTYRENE SULFONATE
52 4SOTALOL HYDROCHLORIDE
53 1SPIRONOLACTONE
54 2TESTOSTERONE
55 5TOPIRAMATE
56 1TROSPIUM CHLORIDE
57 1VALPROIC ACID
58 1VIGABATRIN
59 9WARFARIN SODIUM
60 4ZALEPLON
61 3ZONISAMIDE
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01 22CAPSULE, EXTENDED RELEASE;ORAL
02 27CAPSULE;ORAL
03 1EMULSION;OPHTHALMIC
04 1FOR SOLUTION;ORAL
05 1GEL, METERED;TRANSDERMAL
06 1GEL;TRANSDERMAL
07 4POWDER;ORAL
08 1POWDER;ORAL, RECTAL
09 1POWDER;TOPICAL
10 3SOLUTION/DROPS;OPHTHALMIC
11 1SOLUTION;ORAL
12 1SPRAY, METERED;NASAL
13 1SUSPENSION;ORAL
14 3TABLET, DELAYED RELEASE;ORAL
15 6TABLET, EXTENDED RELEASE;ORAL
16 92TABLET;ORAL
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01 10.025MG;2.5MG
02 10.05%
03 10.15%
04 10.2%;EQ 0.5% BASE
05 10.5MG
06 10.75MG
07 11.5MG
08 1100,000 UNITS/GM
09 10100MG
10 310MEQ
11 1710MG
12 112.5MG/1.25GM ACTUATION
13 2120MG
14 1150MG
15 115MEQ
16 215MG
17 2160MG
18 118MG
19 31MG
20 32.5MG
21 12.5MG/ML
22 1200 IU/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
23 6200MG
24 220MEQ
25 620MG
26 1225MG
27 1240MG
28 1250MG
29 1125MG
30 125MG;25MG
31 22MG
32 2300MG
33 830MG
34 1325MG
35 1325MG;10MG
36 1325MG;5MG
37 1325MG;7.5MG
38 135MG
39 136MG
40 13MG
41 4400MG
42 340MG
43 1425MG
44 1453.6GM/BOT
45 145MG
46 24MG
47 3500MG
48 950MG
49 150MG/5GM PACKET
50 95MG
51 360MG
52 26MG
53 17.5MG
54 1750MG
55 175MG
56 1800MG
57 380MG
58 28MEQ
59 1EQ 0.5% BASE
60 1EQ 10MG BASE
61 1EQ 125MG VALPROIC ACID
62 1EQ 20MG BASE
63 1EQ 20MG BASE/5ML
64 1EQ 250MG VALPROIC ACID
65 1EQ 30MG BASE
66 1EQ 40MG BASE
67 2EQ 4GM RESIN/PACKET
68 2EQ 4GM RESIN/SCOOPFUL
69 1EQ 500MG VALPROIC ACID
70 1EQ 84MG BASE
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01 73DISCN
02 93RX
RLD : No
TE Code :
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET; ORAL
Proprietary Name : HYDROCODONE BITARTRATE A...
Dosage Strength : 325MG;5MG
Approval Date : 2017-03-24
Application Number : 206484
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 : 325MG;7.5MG
Approval Date : 2017-03-24
Application Number : 206484
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 : 325MG;10MG
Approval Date : 2017-03-24
Application Number : 206484
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code : AB
Dosage Form : CAPSULE; ORAL
Proprietary Name : AMANTADINE HYDROCHLORIDE
Dosage Strength : 100MG
Approval Date : 1986-08-05
Application Number : 70589
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : AMANTADINE HYDROCHLORIDE
Dosage Strength : 100MG
Approval Date : 2002-12-16
Application Number : 76186
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : PACERONE
Dosage Strength : 200MG
Approval Date : 1998-04-30
Application Number : 75135
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : PACERONE
Dosage Strength : 100MG
Approval Date : 2005-04-12
Application Number : 75135
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : PACERONE
Dosage Strength : 400MG
Approval Date : 2020-07-02
Application Number : 75135
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : AMIODARONE HYDROCHLORIDE
Dosage Strength : 200MG
Approval Date : 1998-12-23
Application Number : 75315
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : AMIODARONE HYDROCHLORIDE
Dosage Strength : 400MG
Approval Date : 2000-06-30
Application Number : 75315
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
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