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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 2DOXYCYCLINE HYCLATE
26 1DOXYLAMINE SUCCINATE; PYRIDOXINE HYDROCHLORIDE
27 3DROXIDOPA
28 1ENALAPRIL MALEATE
29 1ERGOCALCIFEROL
30 2ESOMEPRAZOLE MAGNESIUM
31 1ETHOSUXIMIDE
32 2FEBUXOSTAT
33 1FINGOLIMOD HYDROCHLORIDE
34 5FLUVOXAMINE MALEATE
35 3GRANISETRON HYDROCHLORIDE
36 1HYDROXYZINE HYDROCHLORIDE
37 2IBUPROFEN
38 2IVABRADINE HYDROCHLORIDE
39 1KETOROLAC TROMETHAMINE
40 1LEVETIRACETAM
41 1LIDOCAINE HYDROCHLORIDE
42 3LOPERAMIDE HYDROCHLORIDE
43 1LOPERAMIDE HYDROCHLORIDE; SIMETHICONE
44 1LORATADINE
45 1LORATADINE; PSEUDOEPHEDRINE SULFATE
46 1MAGNESIUM SULFATE; POTASSIUM SULFATE; SODIUM SULFATE
47 1METFORMIN HYDROCHLORIDE
48 2METHIMAZOLE
49 3METHYLPHENIDATE HYDROCHLORIDE
50 1NAPROXEN SODIUM
51 2NICARDIPINE HYDROCHLORIDE
52 1NIMODIPINE
53 1OXCARBAZEPINE
54 3OXYBUTYNIN CHLORIDE
55 3PARICALCITOL
56 2POTASSIUM CITRATE
57 2PROCHLORPERAZINE MALEATE
58 2PROGESTERONE
59 1RUFINAMIDE
60 1SEVELAMER CARBONATE
61 4TERAZOSIN HYDROCHLORIDE
62 2TETRABENAZINE
63 2THEOPHYLLINE
64 4VALPROIC ACID
65 3ZONISAMIDE
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01 2CAPSULE, DELAYED REL PELLETS;ORAL
02 3CAPSULE, DELAYED RELEASE;ORAL
03 2CAPSULE, EXTENDED RELEASE;ORAL
04 47CAPSULE;ORAL
05 1FOR SUSPENSION;ORAL
06 3INJECTABLE;INJECTION
07 1JELLY;TOPICAL
08 5SOLUTION;ORAL
09 1SPRAY, METERED;NASAL
10 4SUSPENSION;ORAL
11 2SYRUP;ORAL
12 1TABLET, DELAYED RELEASE;ORAL
13 8TABLET, EXTENDED RELEASE;ORAL
14 3TABLET, FOR SUSPENSION;ORAL
15 40TABLET;ORAL
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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/5ML
13 110MG;10MG
14 110MG;240MG
15 112.5MG
16 1125MG
17 1125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
18 1150MG
19 115MEQ
20 115MG
21 11MCG
22 11MG
23 11MG/ML
24 12%
25 12.5MG
26 12.5MG/ML
27 6200MG
28 420MG
29 3250MG
30 1250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
31 1250MG;125MG
32 425MG
33 125MG;EQ 200MG FREE ACID AND POTASSIUM SALT
34 12MCG
35 32MG
36 12MG/5ML;10MG/5ML;30MG/5ML
37 12MG;125MG
38 3300MG
39 1300MG/5ML
40 330MG
41 1400MG
42 140MG
43 140MG/ML
44 1450MG
45 14MCG
46 14MG
47 150,000 IU
48 1500MG
49 1500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
50 1500MG/5ML
51 250MG
52 85MG
53 15MG/5ML
54 1625MG
55 16MG
56 1750MG/5ML
57 175MG
58 1800MG
59 1800MG/PACKET
60 180MG
61 1EQ 0.1MG BASE/ML (EQ 0.1MG BASE/ML)
62 1EQ 0.5MG BASE
63 1EQ 100MG BASE
64 2EQ 10MG BASE
65 1EQ 1MG BASE
66 1EQ 1MG BASE/ML (EQ 1MG BASE/ML)
67 1EQ 200MG BASE
68 1EQ 200MG FREE ACID AND POTASSIUM SALT
69 1EQ 20MG BASE
70 1EQ 250MG BASE
71 1EQ 2MG BASE
72 1EQ 40MG BASE
73 1EQ 4MG BASE/4ML (EQ 1MG BASE/ML)
74 1EQ 500MG BASE
75 1EQ 50MG BASE
76 3EQ 5MG BASE
77 1EQ 600MG BASE
78 1EQ 7.5MG BASE
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01 14DISCN
02 14OTC
03 93RX
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 :
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 : DISCN
RLD : No
TE Code :
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
Huhtamaki is a supplier offers 3 products (APIs, Excipients or Intermediates).
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