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01 2ACETAMINOPHEN; BUTALBITAL
02 3ACETAMINOPHEN; BUTALBITAL; CAFFEINE
03 1ALBUTEROL SULFATE
04 3BENZTROPINE MESYLATE
05 1CETIRIZINE HYDROCHLORIDE
06 1CLINDAMYCIN PHOSPHATE
07 1CLOBETASOL PROPIONATE
08 1CODEINE PHOSPHATE; PROMETHAZINE HYDROCHLORIDE
09 2CYPROHEPTADINE HYDROCHLORIDE
10 5ESTRADIOL
11 3FLUOCINOLONE ACETONIDE
12 1FLUOCINONIDE
13 2GLYCOPYRROLATE
14 1HALOBETASOL PROPIONATE
15 1LEVETIRACETAM
16 1LIDOCAINE
17 7MEPERIDINE HYDROCHLORIDE
18 2METHYLPHENIDATE HYDROCHLORIDE
19 2OXYCODONE HYDROCHLORIDE
20 4PROMETHAZINE HYDROCHLORIDE
21 1PROPYLTHIOURACIL
22 3TRIAMCINOLONE ACETONIDE
23 1VALPROIC ACID
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01 49QUAGEN
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01 2CAPSULE;ORAL
02 1GEL;TOPICAL
03 5GEL;TRANSDERMAL
04 4INJECTABLE;INJECTION
05 2LOTION;TOPICAL
06 1OIL/DROPS;OTIC
07 2OIL;TOPICAL
08 2OINTMENT;TOPICAL
09 1PASTE;DENTAL
10 6SOLUTION;ORAL
11 2SOLUTION;TOPICAL
12 6SYRUP;ORAL
13 15TABLET;ORAL
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01 30.01%
02 10.025%
03 30.05%
04 20.1%
05 10.1% (0.25GM/PACKET)
06 10.1% (0.5GM/PACKET)
07 10.1% (0.75GM/PACKET)
08 10.1% (1.25GM/PACKET)
09 10.1% (1GM/PACKET)
10 10.5MG
11 1100MG
12 1100MG/5ML
13 2100MG/ML
14 110MG/5ML
15 110MG/5ML;6.25MG/5ML
16 112.5MG
17 21MG
18 1250MG/5ML
19 125MG
20 125MG/ML
21 22MG
22 12MG/5ML
23 1300MG;50MG
24 1300MG;50MG;40MG
25 1325MG;50MG
26 2325MG;50MG;40MG
27 14MG
28 15%
29 250MG
30 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
31 150MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
32 150MG/ML
33 35MG/5ML
34 16.25MG/5ML
35 175MG/ML
36 1EQ 1% BASE
37 1EQ 2MG BASE/5ML
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01 49USA
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
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
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
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
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
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
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BENZTROPINE MESYLATE
Dosage Strength : 0.5MG
Packaging :
Approval Date : 2025-02-11
Application Number : 212694
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BENZTROPINE MESYLATE
Dosage Strength : 1MG
Packaging :
Approval Date : 2025-02-11
Application Number : 212694
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BENZTROPINE MESYLATE
Dosage Strength : 2MG
Packaging :
Approval Date : 2025-02-11
Application Number : 212694
Regulatory Info : RX
Registration Country : USA
Regulatory Info : OTC
Registration Country : USA
Dosage Form : SOLUTION;ORAL
Brand Name : CHILDRENS CETIRIZINE HYDR...
Dosage Strength : 5MG/5ML
Packaging :
Approval Date : 2019-05-16
Application Number : 212266
Regulatory Info : OTC
Registration Country : USA