01 1ACETAMINOPHEN; IBUPROFEN
02 1AMANTADINE HYDROCHLORIDE
03 2AMPHETAMINE SULFATE
04 2APIXABAN
05 1ATOVAQUONE
06 1AZELASTINE HYDROCHLORIDE
07 3AZITHROMYCIN
08 2BENZONATATE
09 1BEXAROTENE
10 1BROMPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
11 2CALCITRIOL
12 1CARBAMAZEPINE
13 5CETIRIZINE HYDROCHLORIDE
14 1CEVIMELINE HYDROCHLORIDE
15 4CIMETIDINE
16 3CLOBAZAM
17 1COLESEVELAM HYDROCHLORIDE
18 3DEFERASIROX
19 3DEXAMETHASONE
20 2DEXMETHYLPHENIDATE HYDROCHLORIDE
21 1DICLOFENAC POTASSIUM
22 1DICYCLOMINE HYDROCHLORIDE
23 1DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN
24 3DOFETILIDE
25 1DOXYLAMINE SUCCINATE; PYRIDOXINE HYDROCHLORIDE
26 3DROXIDOPA
27 1ENALAPRIL MALEATE
28 1ERGOCALCIFEROL
29 2ESOMEPRAZOLE MAGNESIUM
30 1ETHOSUXIMIDE
31 2FEBUXOSTAT
32 1FINGOLIMOD HYDROCHLORIDE
33 5FLUVOXAMINE MALEATE
34 3GRANISETRON HYDROCHLORIDE
35 2IBUPROFEN
36 2IVABRADINE HYDROCHLORIDE
37 1KETOROLAC TROMETHAMINE
38 1LEVETIRACETAM
39 1LIDOCAINE HYDROCHLORIDE
40 3LOPERAMIDE HYDROCHLORIDE
41 1LOPERAMIDE HYDROCHLORIDE; SIMETHICONE
42 1LORATADINE
43 1LORATADINE; PSEUDOEPHEDRINE SULFATE
44 1MAGNESIUM SULFATE; POTASSIUM SULFATE; SODIUM SULFATE
45 2METHIMAZOLE
46 3METHYLPHENIDATE HYDROCHLORIDE
47 1NAPROXEN SODIUM
48 2NICARDIPINE HYDROCHLORIDE
49 1NIMODIPINE
50 1OXCARBAZEPINE
51 3OXYBUTYNIN CHLORIDE
52 3PARICALCITOL
53 2POTASSIUM CITRATE
54 2PROCHLORPERAZINE MALEATE
55 2PROGESTERONE
56 1RUFINAMIDE
57 1SEVELAMER CARBONATE
58 4TERAZOSIN HYDROCHLORIDE
59 2TETRABENAZINE
60 2THEOPHYLLINE
61 4VALPROIC ACID
62 2VARENICLINE TARTRATE
63 3ZONISAMIDE
01 2CAPSULE, DELAYED REL PELLETS;ORAL
02 3CAPSULE, DELAYED RELEASE;ORAL
03 2CAPSULE, EXTENDED RELEASE;ORAL
04 45CAPSULE;ORAL
05 1FOR SUSPENSION;ORAL
06 3INJECTABLE;INJECTION
07 1JELLY;TOPICAL
08 4SOLUTION;ORAL
09 1SPRAY, METERED;NASAL
10 4SUSPENSION;ORAL
11 1SYRUP;ORAL
12 1TABLET, DELAYED RELEASE;ORAL
13 8TABLET, EXTENDED RELEASE;ORAL
14 3TABLET, FOR SUSPENSION;ORAL
15 42TABLET;ORAL
01 10.125MG
02 10.137MG/SPRAY
03 10.25MCG
04 10.25MG
05 10.5MCG
06 10.5MG
07 11.6GM/BOT;3.13GM/BOT;17.5GM/BOT
08 7100MG
09 1100MG/ML
10 110MEQ
11 1010MG
12 110MG;10MG
13 110MG;240MG
14 112.5MG
15 1125MG
16 1125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
17 1150MG
18 115MEQ
19 115MG
20 11MCG
21 11MG
22 11MG/ML
23 12%
24 12.5MG
25 12.5MG/ML
26 6200MG
27 420MG
28 3250MG
29 1250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
30 1250MG;125MG
31 425MG
32 125MG;EQ 200MG FREE ACID AND POTASSIUM SALT
33 12MCG
34 32MG
35 12MG/5ML;10MG/5ML;30MG/5ML
36 12MG;125MG
37 3300MG
38 1300MG/5ML
39 330MG
40 1400MG
41 140MG
42 140MG/ML
43 1450MG
44 14MCG
45 14MG
46 150,000 IU
47 1500MG
48 1500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
49 250MG
50 85MG
51 15MG/5ML
52 1625MG
53 16MG
54 1750MG/5ML
55 175MG
56 1800MG
57 1800MG/PACKET
58 180MG
59 1EQ 0.1MG BASE/ML (EQ 0.1MG BASE/ML)
60 2EQ 0.5MG BASE
61 2EQ 10MG BASE
62 2EQ 1MG BASE
63 1EQ 1MG BASE/ML (EQ 1MG BASE/ML)
64 1EQ 200MG BASE
65 1EQ 200MG FREE ACID AND POTASSIUM SALT
66 1EQ 20MG BASE
67 1EQ 250MG BASE
68 1EQ 2MG BASE
69 1EQ 40MG BASE
70 1EQ 4MG BASE/4ML (EQ 1MG BASE/ML)
71 1EQ 500MG BASE
72 3EQ 5MG BASE
73 1EQ 600MG BASE
74 1EQ 7.5MG BASE
01 9DISCN
02 14OTC
03 92RX
04 6Blank
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : ACETAMINOPHEN AND IBUPRO...
Dosage Strength : 250MG;125MG
Approval Date : 2023-08-01
Application Number : 216999
RX/OTC/DISCN : OTC
RLD : No
TE Code :
RLD : No
TE Code : AB
Dosage Form : CAPSULE; ORAL
Proprietary Name : AMANTADINE HYDROCHLORIDE
Dosage Strength : 100MG
Approval Date : 2008-05-29
Application Number : 78720
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AA
Dosage Form : TABLET; ORAL
Proprietary Name : AMPHETAMINE SULFATE
Dosage Strength : 5MG
Approval Date : 2019-11-22
Application Number : 212919
RX/OTC/DISCN : RX
RLD : No
TE Code : AA
RLD : No
TE Code : AA
Dosage Form : TABLET; ORAL
Proprietary Name : AMPHETAMINE SULFATE
Dosage Strength : 10MG
Approval Date : 2019-11-22
Application Number : 212919
RX/OTC/DISCN : RX
RLD : No
TE Code : AA
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : APIXABAN
Dosage Strength : 2.5MG
Approval Date : 2020-04-08
Application Number : 210152
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : APIXABAN
Dosage Strength : 5MG
Approval Date : 2020-04-08
Application Number : 210152
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code : AB
Dosage Form : SUSPENSION; ORAL
Proprietary Name : ATOVAQUONE
Dosage Strength : 750MG/5ML
Approval Date : 2021-03-30
Application Number : 212918
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : SPRAY, METERED; NASAL
Proprietary Name : AZELASTINE HYDROCHLORIDE
Dosage Strength : 0.137MG/SPRAY
Approval Date : 2015-07-28
Application Number : 90176
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : AZITHROMYCIN
Dosage Strength : EQ 600MG BASE
Approval Date : 2018-12-26
Application Number : 209999
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : AZITHROMYCIN
Dosage Strength : EQ 250MG BASE
Approval Date : 2019-02-26
Application Number : 210000
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
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