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 1ETHOSUXIMIDE
29 1FINGOLIMOD HYDROCHLORIDE
30 5FLUVOXAMINE MALEATE
31 3GRANISETRON HYDROCHLORIDE
32 2IBUPROFEN
33 2IVABRADINE HYDROCHLORIDE
34 1KETOROLAC TROMETHAMINE
35 1LEVETIRACETAM
36 1LIDOCAINE HYDROCHLORIDE
37 3LOPERAMIDE HYDROCHLORIDE
38 1LOPERAMIDE HYDROCHLORIDE; SIMETHICONE
39 1LORATADINE
40 1LORATADINE; PSEUDOEPHEDRINE SULFATE
41 1MAGNESIUM SULFATE; POTASSIUM SULFATE; SODIUM SULFATE
42 2METHIMAZOLE
43 3METHYLPHENIDATE HYDROCHLORIDE
44 1NAPROXEN SODIUM
45 2NICARDIPINE HYDROCHLORIDE
46 1NIMODIPINE
47 1OXCARBAZEPINE
48 3OXYBUTYNIN CHLORIDE
49 3PARICALCITOL
50 2POTASSIUM CITRATE
51 2PROCHLORPERAZINE MALEATE
52 2PROGESTERONE
53 1RUFINAMIDE
54 1SEVELAMER CARBONATE
55 4TERAZOSIN HYDROCHLORIDE
56 2TETRABENAZINE
57 2THEOPHYLLINE
58 4VALPROIC ACID
59 2VARENICLINE TARTRATE
60 3ZONISAMIDE
01 113BIONPHARMA
01 3CAPSULE, DELAYED RELEASE;ORAL
02 2CAPSULE, EXTENDED RELEASE;ORAL
03 45CAPSULE;ORAL
04 1FOR SUSPENSION;ORAL
05 3INJECTABLE;INJECTION
06 1JELLY;TOPICAL
07 4SOLUTION;ORAL
08 1SPRAY, METERED;NASAL
09 4SUSPENSION;ORAL
10 1SYRUP;ORAL
11 1TABLET, DELAYED RELEASE;ORAL
12 8TABLET, EXTENDED RELEASE;ORAL
13 3TABLET, FOR SUSPENSION;ORAL
14 36TABLET;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16 1125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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29 1250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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/ML
41 1450MG
42 14MCG
43 14MG
44 150,000 IU
45 1500MG
46 1500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
47 250MG
48 85MG
49 15MG/5ML
50 1625MG
51 16MG
52 1750MG/5ML
53 175MG
54 1800MG/PACKET
55 1EQ 0.1MG BASE/ML (EQ 0.1MG BASE/ML)
56 2EQ 0.5MG BASE
57 2EQ 10MG BASE
58 2EQ 1MG BASE
59 1EQ 1MG BASE/ML (EQ 1MG BASE/ML)
60 1EQ 200MG BASE
61 1EQ 200MG FREE ACID AND POTASSIUM SALT
62 1EQ 250MG BASE
63 1EQ 2MG BASE
64 1EQ 4MG BASE/4ML (EQ 1MG BASE/ML)
65 1EQ 500MG BASE
66 3EQ 5MG BASE
67 1EQ 600MG BASE
68 1EQ 7.5MG BASE
01 113USA
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 : RX
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 : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : AZITHROMYCIN
Dosage Strength : EQ 600MG BASE
Packaging :
Approval Date : 2018-12-26
Application Number : 209999
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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