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 3CLOBAZAM
16 1COLESEVELAM HYDROCHLORIDE
17 3DEFERASIROX
18 3DEXAMETHASONE
19 2DEXMETHYLPHENIDATE HYDROCHLORIDE
20 1DICLOFENAC POTASSIUM
21 1DICYCLOMINE HYDROCHLORIDE
22 1DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN
23 3DOFETILIDE
24 1DOXYLAMINE SUCCINATE; PYRIDOXINE HYDROCHLORIDE
25 3DROXIDOPA
26 1ENALAPRIL MALEATE
27 1ERGOCALCIFEROL
28 2ESOMEPRAZOLE MAGNESIUM
29 1ETHOSUXIMIDE
30 2FEBUXOSTAT
31 1FINGOLIMOD HYDROCHLORIDE
32 5FLUVOXAMINE MALEATE
33 3GRANISETRON HYDROCHLORIDE
34 2IBUPROFEN
35 2IVABRADINE HYDROCHLORIDE
36 1KETOROLAC TROMETHAMINE
37 1LEVETIRACETAM
38 1LIDOCAINE HYDROCHLORIDE
39 3LOPERAMIDE HYDROCHLORIDE
40 1LOPERAMIDE HYDROCHLORIDE; SIMETHICONE
41 1LORATADINE
42 1LORATADINE; PSEUDOEPHEDRINE SULFATE
43 1MAGNESIUM SULFATE; POTASSIUM SULFATE; SODIUM SULFATE
44 2METHIMAZOLE
45 3METHYLPHENIDATE HYDROCHLORIDE
46 1NAPROXEN SODIUM
47 2NICARDIPINE HYDROCHLORIDE
48 1NIMODIPINE
49 1OXCARBAZEPINE
50 3OXYBUTYNIN CHLORIDE
51 3PARICALCITOL
52 2POTASSIUM CITRATE
53 2PROCHLORPERAZINE MALEATE
54 2PROGESTERONE
55 1RUFINAMIDE
56 1SEVELAMER CARBONATE
57 4TERAZOSIN HYDROCHLORIDE
58 2TETRABENAZINE
59 2THEOPHYLLINE
60 4VALPROIC ACID
61 2VARENICLINE TARTRATE
62 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 38TABLET;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16 1125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 5200MG
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29 1250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 2300MG
38 1300MG/5ML
39 330MG
40 140MG
41 140MG/ML
42 1450MG
43 14MCG
44 14MG
45 150,000 IU
46 1500MG
47 1500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
48 250MG
49 85MG
50 15MG/5ML
51 1625MG
52 16MG
53 1750MG/5ML
54 175MG
55 1800MG/PACKET
56 180MG
57 1EQ 0.1MG BASE/ML (EQ 0.1MG BASE/ML)
58 2EQ 0.5MG BASE
59 2EQ 10MG BASE
60 2EQ 1MG BASE
61 1EQ 1MG BASE/ML (EQ 1MG BASE/ML)
62 1EQ 200MG BASE
63 1EQ 200MG FREE ACID AND POTASSIUM SALT
64 1EQ 20MG BASE
65 1EQ 250MG BASE
66 1EQ 2MG BASE
67 1EQ 40MG BASE
68 1EQ 4MG BASE/4ML (EQ 1MG BASE/ML)
69 1EQ 500MG BASE
70 3EQ 5MG BASE
71 1EQ 600MG BASE
72 1EQ 7.5MG BASE
01 9DISCN
02 14OTC
03 92RX
04 2Blank
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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