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01 2ACETAMINOPHEN; BUTALBITAL
02 3ACETAMINOPHEN; BUTALBITAL; CAFFEINE
03 1ACETAMINOPHEN; BUTALBITAL; CAFFEINE; CODEINE PHOSPHATE
04 1ALBUTEROL SULFATE
05 1ARIPIPRAZOLE
06 2ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE
07 3BENZTROPINE MESYLATE
08 1CETIRIZINE HYDROCHLORIDE
09 1CLOBETASOL PROPIONATE
10 3CLONAZEPAM
11 1CODEINE PHOSPHATE; PROMETHAZINE HYDROCHLORIDE
12 2CYPROHEPTADINE HYDROCHLORIDE
13 3DEXTROAMPHETAMINE SULFATE
14 3FLUOCINOLONE ACETONIDE
15 1FLUOCINONIDE
16 3FLUVOXAMINE MALEATE
17 3GLIMEPIRIDE
18 3GLYCOPYRROLATE
19 1HALOBETASOL PROPIONATE
20 1HYDROCHLOROTHIAZIDE
21 1LEVETIRACETAM
22 1LIDOCAINE
23 1LIDOCAINE HYDROCHLORIDE
24 7MEPERIDINE HYDROCHLORIDE
25 1MESALAMINE
26 1METHENAMINE HIPPURATE
27 3METHYLDOPA
28 5METHYLPHENIDATE HYDROCHLORIDE
29 3MEXILETINE HYDROCHLORIDE
30 2OXYCODONE HYDROCHLORIDE
31 2POTASSIUM CHLORIDE
32 4PROMETHAZINE HYDROCHLORIDE
33 1PROPYLTHIOURACIL
34 3REPAGLINIDE
35 1RITONAVIR
36 2SELEGILINE HYDROCHLORIDE
37 3SERTRALINE HYDROCHLORIDE
38 3TRIAMCINOLONE ACETONIDE
39 1URSODIOL
40 1VALPROIC ACID
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01 85QUAGEN
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01 3CAPSULE, EXTENDED RELEASE;ORAL
02 10CAPSULE;ORAL
03 4INJECTABLE;INJECTION
04 2LOTION;TOPICAL
05 1OIL/DROPS;OTIC
06 2OIL;TOPICAL
07 2OINTMENT;TOPICAL
08 1PASTE;DENTAL
09 11SOLUTION;ORAL
10 2SOLUTION;TOPICAL
11 1SUPPOSITORY;RECTAL
12 6SYRUP;ORAL
13 3TABLET, CHEWABLE;ORAL
14 37TABLET;ORAL
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01 30.01%
02 10.025%
03 20.025MG;2.5MG
04 30.05%
05 20.1%
06 30.5MG
07 2100MG
08 1100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
09 1100MG/5ML
10 2100MG/ML
11 210MG
12 110MG/5ML
13 110MG/5ML;6.25MG/5ML
14 212.5MG
15 1125MG
16 1150MG
17 115MG
18 21GM
19 51MG
20 11MG/5ML
21 11MG/ML
22 12%
23 12.5MG
24 1200MG
25 120MEQ/15ML
26 2250MG
27 1250MG/5ML
28 225MG
29 125MG/ML
30 52MG
31 12MG/5ML
32 1300MG
33 1300MG;50MG
34 1300MG;50MG;40MG
35 1325MG;50MG
36 2325MG;50MG;40MG
37 1325MG;50MG;40MG;30MG
38 140MEQ/15ML
39 24MG
40 15%
41 1500MG
42 350MG
43 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
44 150MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
45 150MG/ML
46 25MG
47 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
48 35MG/5ML
49 16.25MG/5ML
50 175MG/ML
51 1EQ 100MG BASE
52 1EQ 25MG BASE
53 1EQ 2MG BASE/5ML
54 1EQ 50MG BASE
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01 85USA
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Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BUTALBITAL AND ACETAMINOP...
Dosage Strength : 325MG;50MG
Packaging :
Approval Date : 2024-01-18
Application Number : 214291
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 : 2024-02-01
Application Number : 214305
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Dosage Form : TABLET;ORAL
Brand Name : BUTALBITAL, ACETAMINOPHEN...
Dosage Strength : 325MG;50MG;40MG
Packaging :
Approval Date : 2024-01-18
Application Number : 214287
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Dosage Form : CAPSULE;ORAL
Brand Name : BUTALBITAL, ACETAMINOPHEN...
Dosage Strength : 300MG;50MG;40MG
Packaging :
Approval Date : 2024-02-08
Application Number : 214288
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Dosage Form : CAPSULE;ORAL
Brand Name : BUTALBITAL, ACETAMINOPHEN...
Dosage Strength : 325MG;50MG;40MG
Packaging :
Approval Date : 2024-03-12
Application Number : 216376
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
ACETAMINOPHEN; BUTALBITAL; CAFFEINE; CODEINE PHOSPHATE
Dosage Form : CAPSULE;ORAL
Brand Name : BUTALBITAL, ACETAMINOPHEN...
Dosage Strength : 325MG;50MG;40MG;30MG
Packaging :
Approval Date : 2020-07-08
Application Number : 204649
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : SYRUP;ORAL
Brand Name : ALBUTEROL SULFATE
Dosage Strength : EQ 2MG BASE/5ML
Packaging :
Approval Date : 2019-09-06
Application Number : 212197
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION;ORAL
Brand Name : ARIPIPRAZOLE
Dosage Strength : 1MG/ML
Packaging :
Approval Date : 2025-10-22
Application Number : 215582
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Brand Name : DIPHENOXYLATE HYDROCHLORI...
Dosage Strength : 0.025MG;2.5MG
Packaging :
Approval Date : 1982-01-01
Application Number : 85762
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Brand Name : DIPHENOXYLATE HYDROCHLORI...
Dosage Strength : 0.025MG;2.5MG
Packaging :
Approval Date : 2018-08-31
Application Number : 210571
Regulatory Info : DISCN
Registration Country : USA
