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01 2ACETAMINOPHEN; BUTALBITAL
02 1CAFFEINE; ERGOTAMINE TARTRATE
03 1CALCITRIOL
04 3CANDESARTAN CILEXETIL; HYDROCHLOROTHIAZIDE
05 3CEFDINIR
06 2CEFPODOXIME PROXETIL
07 1CEFTRIAXONE SODIUM
08 3CEFUROXIME AXETIL
09 2CEPHALEXIN
10 4CHLORZOXAZONE
11 1DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM
12 1ETODOLAC
13 1FLUOCINOLONE ACETONIDE
14 3GALANTAMINE HYDROBROMIDE
15 1HYDROXYCHLOROQUINE SULFATE
16 6LEVETIRACETAM
17 1LORATADINE
18 2METHAZOLAMIDE
19 2METHYLPHENIDATE HYDROCHLORIDE
20 2MONTELUKAST SODIUM
21 6MORPHINE SULFATE
22 2NICARDIPINE HYDROCHLORIDE
23 2OMEPRAZOLE; SODIUM BICARBONATE
24 3POTASSIUM CHLORIDE
25 2PRASUGREL HYDROCHLORIDE
26 1PREGABALIN
27 4PROPRANOLOL HYDROCHLORIDE
28 4RAMIPRIL
29 2TIZANIDINE HYDROCHLORIDE
30 6TOPIRAMATE
31 3TRANDOLAPRIL
32 2ZOLPIDEM TARTRATE
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01 79ANDA REPOSITORY
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01 10CAPSULE, EXTENDED RELEASE;ORAL
02 15CAPSULE;ORAL
03 1FOR SOLUTION;ORAL
04 2FOR SUSPENSION;ORAL
05 1INJECTABLE;INJECTION
06 1OIL/DROPS;OTIC
07 6SOLUTION;ORAL
08 1SOLUTION;ORAL, RECTAL
09 2TABLET, CHEWABLE;ORAL
10 2TABLET, EXTENDED RELEASE;ORAL
11 38TABLET;ORAL
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01 10.01%
02 11.25MG
03 2100MG
04 1100MG;1MG
05 310MG
06 110MG/5ML
07 1120MG
08 1125MG/5ML
09 115MG
10 1160MG
11 116MG;12.5MG
12 11GM
13 11MCG/ML
14 11MG
15 12.5MG
16 2200MG
17 120MEQ
18 120MEQ/15ML
19 220MG
20 120MG/ML
21 120MG;1.1GM
22 2250MG
23 1250MG/5ML
24 325MG
25 12MG
26 1300MG
27 1300MG;50MG
28 230MG
29 1325MG;50MG
30 132MG;12.5MG
31 132MG;25MG
32 1375MG
33 1400MG
34 140MEQ/15ML
35 140MG;1.1GM
36 14MG
37 3500MG
38 350MG
39 25MG
40 15MG/5ML
41 260MG
42 166%;10%
43 3750MG
44 280MG
45 1EQ 100MG BASE
46 1EQ 10GM BASE/VIAL
47 1EQ 10MG BASE
48 1EQ 125MG BASE
49 1EQ 12MG BASE
50 1EQ 200MG BASE
51 2EQ 250MG BASE
52 3EQ 4MG BASE
53 2EQ 500MG BASE
54 2EQ 5MG BASE
55 1EQ 6MG BASE
56 1EQ 8MG BASE
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01 79USA
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Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BUTAPAP
Dosage Strength : 325MG;50MG
Packaging :
Approval Date : 1992-10-26
Application Number : 89987
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BUTALBITAL AND ACETAMINOP...
Dosage Strength : 300MG;50MG
Packaging :
Approval Date : 2016-11-15
Application Number : 207386
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ERGOTAMINE TARTRATE AND C...
Dosage Strength : 100MG;1MG
Packaging :
Approval Date : 2005-09-16
Application Number : 40590
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION;ORAL
Brand Name : CALCITRIOL
Dosage Strength : 1MCG/ML
Packaging :
Approval Date : 2023-07-28
Application Number : 203973
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
CANDESARTAN CILEXETIL; HYDROCHLOROTHIAZIDE
Dosage Form : TABLET;ORAL
Brand Name : CANDESARTAN CILEXETIL AND...
Dosage Strength : 16MG;12.5MG
Packaging :
Approval Date : 2013-06-03
Application Number : 202965
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
CANDESARTAN CILEXETIL; HYDROCHLOROTHIAZIDE
Dosage Form : TABLET;ORAL
Brand Name : CANDESARTAN CILEXETIL AND...
Dosage Strength : 32MG;12.5MG
Packaging :
Approval Date : 2013-06-03
Application Number : 202965
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
CANDESARTAN CILEXETIL; HYDROCHLOROTHIAZIDE
Dosage Form : TABLET;ORAL
Brand Name : CANDESARTAN CILEXETIL AND...
Dosage Strength : 32MG;25MG
Packaging :
Approval Date : 2013-06-03
Application Number : 202965
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : CAPSULE;ORAL
Brand Name : CEFDINIR
Dosage Strength : 300MG
Packaging :
Approval Date : 2007-07-18
Application Number : 65418
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : FOR SUSPENSION;ORAL
Brand Name : CEFDINIR
Dosage Strength : 125MG/5ML
Packaging :
Approval Date : 2007-07-18
Application Number : 65429
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : FOR SUSPENSION;ORAL
Brand Name : CEFDINIR
Dosage Strength : 250MG/5ML
Packaging :
Approval Date : 2007-07-18
Application Number : 65429
Regulatory Info : RX
Registration Country : USA
