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01 1ALBENDAZOLE
02 3BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE
03 6BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
04 1CARBIDOPA
05 1COLESTIPOL HYDROCHLORIDE
06 4DILTIAZEM HYDROCHLORIDE
07 2GLYCOPYRROLATE
08 1IVERMECTIN
09 1LOPERAMIDE HYDROCHLORIDE
10 1MIGLUSTAT
11 2Methenamine Mandelate
12 4PREDNISOLONE SODIUM PHOSPHATE
13 2TINIDAZOLE
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01 27EDENBRIDGE PHARMS
02 2Edenbridge Pharmaceuticals
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01 2CAPSULE;ORAL
02 4SOLUTION;ORAL
03 2TABLET, ORALLY DISINTEGRATING;ORAL
04 13TABLET;ORAL
05 6TABLET;SUBLINGUAL
06 2Tablet
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01 10.85MG
02 11.7MG
03 11000MG
04 1100MG
05 110MG;6.25MG
06 1120MG
07 11GM
08 12.5MG;6.25MG
09 1200MG
10 1250MG
11 125MG
12 12MG
13 130MG
14 13MG
15 2500MG
16 15MG;6.25MG
17 160MG
18 190MG
19 1EQ 0.7MG BASE;EQ 0.18MG BASE
20 1EQ 1.4MG BASE;EQ 0.36MG BASE
21 1EQ 10MG BASE/5ML
22 1EQ 11.4MG BASE;EQ 2.9MG BASE
23 1EQ 15MG BASE/5ML
24 1EQ 2.9MG BASE;EQ 0.71MG BASE
25 1EQ 20MG BASE/5ML
26 1EQ 25MG BASE/5ML
27 1EQ 5.7MG BASE;EQ 1.4MG BASE
28 1EQ 8.6MG BASE;EQ 2.1MG BASE
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01 2U.S.A
02 27USA
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Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ALBENDAZOLE
Dosage Strength : 200MG
Packaging :
Approval Date : 2019-05-14
Application Number : 211117
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE
Dosage Form : TABLET;ORAL
Brand Name : BISOPROLOL FUMARATE AND H...
Dosage Strength : 2.5MG;6.25MG
Packaging :
Approval Date : 2020-07-09
Application Number : 212678
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE
Dosage Form : TABLET;ORAL
Brand Name : BISOPROLOL FUMARATE AND H...
Dosage Strength : 5MG;6.25MG
Packaging :
Approval Date : 2020-07-09
Application Number : 212678
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE
Dosage Form : TABLET;ORAL
Brand Name : BISOPROLOL FUMARATE AND H...
Dosage Strength : 10MG;6.25MG
Packaging :
Approval Date : 2020-07-09
Application Number : 212678
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
Dosage Form : TABLET;SUBLINGUAL
Brand Name : ZUBSOLV
Dosage Strength : EQ 1.4MG BASE;EQ 0.36M...
Packaging :
Approval Date : 2013-07-03
Application Number : 204242
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
Dosage Form : TABLET;SUBLINGUAL
Brand Name : ZUBSOLV
Dosage Strength : EQ 5.7MG BASE;EQ 1.4MG...
Packaging :
Approval Date : 2013-07-03
Application Number : 204242
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
Dosage Form : TABLET;SUBLINGUAL
Brand Name : ZUBSOLV
Dosage Strength : EQ 8.6MG BASE;EQ 2.1MG...
Packaging :
Approval Date : 2014-12-11
Application Number : 204242
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
Dosage Form : TABLET;SUBLINGUAL
Brand Name : ZUBSOLV
Dosage Strength : EQ 11.4MG BASE;EQ 2.9M...
Packaging :
Approval Date : 2014-12-11
Application Number : 204242
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
Dosage Form : TABLET;SUBLINGUAL
Brand Name : ZUBSOLV
Dosage Strength : EQ 2.9MG BASE;EQ 0.71M...
Packaging :
Approval Date : 2015-06-04
Application Number : 204242
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
Dosage Form : TABLET;SUBLINGUAL
Brand Name : ZUBSOLV
Dosage Strength : EQ 0.7MG BASE;EQ 0.18M...
Packaging :
Approval Date : 2016-10-04
Application Number : 204242
Regulatory Info : RX
Registration Country : USA
