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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 1ETHOSUXIMIDE
31 1FAMOTIDINE
32 1FINGOLIMOD HYDROCHLORIDE
33 5FLUVOXAMINE MALEATE
34 3GRANISETRON HYDROCHLORIDE
35 1HYDROXYZINE HYDROCHLORIDE
36 2IBUPROFEN
37 2IVABRADINE HYDROCHLORIDE
38 1KETOROLAC TROMETHAMINE
39 1LEVETIRACETAM
40 1LIDOCAINE HYDROCHLORIDE
41 3LOPERAMIDE HYDROCHLORIDE
42 1LOPERAMIDE HYDROCHLORIDE; SIMETHICONE
43 1LORATADINE
44 1LORATADINE; PSEUDOEPHEDRINE SULFATE
45 1MAGNESIUM SULFATE; POTASSIUM SULFATE; SODIUM SULFATE
46 1METFORMIN HYDROCHLORIDE
47 2METHIMAZOLE
48 3METHYLPHENIDATE HYDROCHLORIDE
49 1NAPROXEN SODIUM
50 2NICARDIPINE HYDROCHLORIDE
51 1NIMODIPINE
52 1OXCARBAZEPINE
53 3OXYBUTYNIN CHLORIDE
54 3PARICALCITOL
55 2POTASSIUM CITRATE
56 2PROCHLORPERAZINE MALEATE
57 2PROGESTERONE
58 1RUFINAMIDE
59 1SEVELAMER CARBONATE
60 4TERAZOSIN HYDROCHLORIDE
61 2TETRABENAZINE
62 2THEOPHYLLINE
63 4VALPROIC ACID
64 3ZONISAMIDE
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01 120BIONPHARMA
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01 3CAPSULE, DELAYED RELEASE;ORAL
02 2CAPSULE, EXTENDED RELEASE;ORAL
03 47CAPSULE;ORAL
04 2FOR SUSPENSION;ORAL
05 3INJECTABLE;INJECTION
06 1JELLY;TOPICAL
07 5SOLUTION;ORAL
08 1SPRAY, METERED;NASAL
09 4SUSPENSION;ORAL
10 2SYRUP;ORAL
11 1TABLET, DELAYED RELEASE;ORAL
12 8TABLET, EXTENDED RELEASE;ORAL
13 3TABLET, FOR SUSPENSION;ORAL
14 38TABLET;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17 1125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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/5ML
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 1EQ 0.1MG BASE/ML (EQ 0.1MG BASE/ML)
61 1EQ 0.5MG BASE
62 1EQ 100MG BASE
63 2EQ 10MG BASE
64 1EQ 1MG BASE
65 1EQ 1MG BASE/ML (EQ 1MG BASE/ML)
66 1EQ 200MG BASE
67 1EQ 200MG FREE ACID AND POTASSIUM SALT
68 1EQ 250MG BASE
69 1EQ 2MG BASE
70 1EQ 4MG BASE/4ML (EQ 1MG BASE/ML)
71 1EQ 500MG BASE
72 1EQ 50MG BASE
73 3EQ 5MG BASE
74 1EQ 600MG BASE
75 1EQ 7.5MG BASE
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01 120USA
Regulatory Info : OTC
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ACETAMINOPHEN AND IBUPROF...
Dosage Strength : 250MG;125MG
Packaging :
Approval Date : 2023-08-01
Application Number : 216999
Regulatory Info : OTC
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : CAPSULE;ORAL
Brand Name : AMANTADINE HYDROCHLORIDE
Dosage Strength : 100MG
Packaging :
Approval Date : 2008-05-29
Application Number : 78720
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : AMPHETAMINE SULFATE
Dosage Strength : 5MG
Packaging :
Approval Date : 2019-11-22
Application Number : 212919
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : AMPHETAMINE SULFATE
Dosage Strength : 10MG
Packaging :
Approval Date : 2019-11-22
Application Number : 212919
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : APIXABAN
Dosage Strength : 2.5MG
Packaging :
Approval Date : 2020-04-08
Application Number : 210152
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : APIXABAN
Dosage Strength : 5MG
Packaging :
Approval Date : 2020-04-08
Application Number : 210152
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SUSPENSION;ORAL
Brand Name : ATOVAQUONE
Dosage Strength : 750MG/5ML
Packaging :
Approval Date : 2021-03-30
Application Number : 212918
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : SPRAY, METERED;NASAL
Brand Name : AZELASTINE HYDROCHLORIDE
Dosage Strength : 0.137MG/SPRAY
Packaging :
Approval Date : 2015-07-28
Application Number : 90176
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : AZITHROMYCIN
Dosage Strength : EQ 250MG BASE
Packaging :
Approval Date : 2019-02-26
Application Number : 210000
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : AZITHROMYCIN
Dosage Strength : EQ 500MG BASE
Packaging :
Approval Date : 2019-02-26
Application Number : 210001
Regulatory Info : RX
Registration Country : USA
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