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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 2BRIMONIDINE TARTRATE
08 1BRIMONIDINE TARTRATE; TIMOLOL MALEATE
09 1BROMPHENIRAMINE MALEATE
10 3BUMETANIDE
11 1CALCITONIN SALMON RECOMBINANT
12 3CHLORDIAZEPOXIDE HYDROCHLORIDE
13 5CHLORPROMAZINE HYDROCHLORIDE
14 4CIMETIDINE
15 3CLOBAZAM
16 5DEFLAZACORT
17 2DEXAMETHASONE
18 1DIFLUPREDNATE
19 3DIVALPROEX SODIUM
20 3DROXIDOPA
21 1ELIGLUSTAT TARTRATE
22 1ETHACRYNIC ACID
23 1EXEMESTANE
24 1FLUOXETINE HYDROCHLORIDE
25 1FLUOXYMESTERONE
26 4FLUPHENAZINE HYDROCHLORIDE
27 3FLUVOXAMINE MALEATE
28 3FOSINOPRIL SODIUM
29 1GLUTETHIMIDE
30 4HYDRALAZINE HYDROCHLORIDE
31 1HYDROCHLOROTHIAZIDE; SPIRONOLACTONE
32 8ISOTRETINOIN
33 1MEDROXYPROGESTERONE ACETATE
34 2MEMANTINE HYDROCHLORIDE
35 2METHOCARBAMOL
36 3MIRTAZAPINE
37 9MORPHINE SULFATE
38 1MOXIFLOXACIN HYDROCHLORIDE
39 1NYSTATIN
40 2OXANDROLONE
41 4PAROXETINE HYDROCHLORIDE
42 1PENTOXIFYLLINE
43 1PHENDIMETRAZINE TARTRATE
44 2PHENTERMINE HYDROCHLORIDE
45 8POTASSIUM CHLORIDE
46 2PREDNISONE
47 3PROPAFENONE HYDROCHLORIDE
48 4PROPRANOLOL HYDROCHLORIDE
49 1SODIUM POLYSTYRENE SULFONATE
50 4SOTALOL HYDROCHLORIDE
51 1SPIRONOLACTONE
52 2TESTOSTERONE
53 5TOPIRAMATE
54 1TROSPIUM CHLORIDE
55 1VALPROIC ACID
56 1VIGABATRIN
57 9WARFARIN SODIUM
58 4ZALEPLON
59 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 1POWDER;ORAL, RECTAL
08 1POWDER;TOPICAL
09 4SOLUTION/DROPS;OPHTHALMIC
10 1SOLUTION;ORAL
11 1SPRAY, METERED;NASAL
12 2SUSPENSION;ORAL
13 3TABLET, DELAYED RELEASE;ORAL
14 6TABLET, EXTENDED RELEASE;ORAL
15 88TABLET;ORAL
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01 10.025MG;2.5MG
02 10.05%
03 10.1%
04 10.15%
05 10.2%;EQ 0.5% BASE
06 10.5MG
07 10.75MG
08 11.5MG
09 1100,000 UNITS/GM
10 9100MG
11 310MEQ
12 1710MG
13 112.5MG/1.25GM ACTUATION
14 2120MG
15 1150MG
16 115MEQ
17 215MG
18 2160MG
19 118MG
20 31MG
21 32.5MG
22 12.5MG/ML
23 1200 IU/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
24 6200MG
25 220MEQ
26 620MG
27 122.75MG/ML
28 1225MG
29 1240MG
30 1250MG
31 1025MG
32 125MG;25MG
33 22MG
34 2300MG
35 830MG
36 1325MG
37 1325MG;10MG
38 1325MG;5MG
39 1325MG;7.5MG
40 135MG
41 136MG
42 13MG
43 4400MG
44 340MG
45 1425MG
46 1453.6GM/BOT
47 145MG
48 24MG
49 3500MG
50 850MG
51 150MG/5GM PACKET
52 85MG
53 360MG
54 26MG
55 17.5MG
56 1750MG
57 175MG
58 1800MG
59 380MG
60 28MEQ
61 1EQ 0.5% BASE
62 1EQ 10MG BASE
63 1EQ 125MG VALPROIC ACID
64 1EQ 20MG BASE
65 1EQ 20MG BASE/5ML
66 1EQ 250MG VALPROIC ACID
67 1EQ 30MG BASE
68 1EQ 40MG BASE
69 1EQ 500MG VALPROIC ACID
70 1EQ 84MG BASE
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01 71DISCN
02 88RX
03 1Blank
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 :
Upsher-smith Laboratories is a supplier offers 2 products (APIs, Excipients or Intermediates).
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