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01 3ACETAMINOPHEN; HYDROCODONE BITARTRATE
02 1AMANTADINE HYDROCHLORIDE
03 1BROMPHENIRAMINE MALEATE
04 1BROMPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
05 5CEFOTETAN DISODIUM
06 4CEFTAZIDIME
07 3CEFTAZIDIME SODIUM
08 5CEFUROXIME SODIUM
09 3CETIRIZINE HYDROCHLORIDE
10 1CHLORHEXIDINE GLUCONATE
11 1CHLORPHENIRAMINE MALEATE
12 2CHLORPROMAZINE HYDROCHLORIDE
13 3CIMETIDINE HYDROCHLORIDE
14 1CITALOPRAM HYDROBROMIDE
15 1CLINDAMYCIN PHOSPHATE
16 3CLOBETASOL PROPIONATE
17 2CODEINE PHOSPHATE; PROMETHAZINE HYDROCHLORIDE
18 1CYCLOSPORINE
19 1CYPROHEPTADINE HYDROCHLORIDE
20 2DESONIDE
21 1DESOXIMETASONE
22 1DEXCHLORPHENIRAMINE MALEATE
23 1DICLOFENAC SODIUM
24 1DIPHENHYDRAMINE HYDROCHLORIDE
25 1DOXEPIN HYDROCHLORIDE
26 2EDROPHONIUM CHLORIDE
27 1ERYTHROMYCIN
28 1ETHOSUXIMIDE
29 1FLUOCINOLONE ACETONIDE
30 2FLUOCINONIDE
31 1FLUOXETINE HYDROCHLORIDE
32 2FLUPHENAZINE HYDROCHLORIDE
33 1GABAPENTIN
34 1HALOPERIDOL LACTATE
35 2HYDROCORTISONE
36 1HYDROXYZINE HYDROCHLORIDE
37 2IBUPROFEN
38 2LACTULOSE
39 1LEVETIRACETAM
40 2LIDOCAINE HYDROCHLORIDE
41 1LIDOCAINE; PRILOCAINE
42 1LITHIUM CITRATE
43 2LORATADINE
44 1LORAZEPAM
45 1MIDAZOLAM HYDROCHLORIDE
46 2MORPHINE SULFATE
47 1NORTRIPTYLINE HYDROCHLORIDE
48 1NYSTATIN
49 1NYSTATIN; TRIAMCINOLONE ACETONIDE
50 1ONDANSETRON HYDROCHLORIDE
51 1ORPHENADRINE CITRATE
52 2OXYBUTYNIN CHLORIDE
53 2OXYCODONE HYDROCHLORIDE
54 1PERPHENAZINE
55 1PHENYTOIN
56 2PHYTONADIONE
57 2POTASSIUM CHLORIDE
58 3PREDNISOLONE
59 5PREDNISOLONE SODIUM PHOSPHATE
60 2PROMETHAZINE HYDROCHLORIDE
61 2PROPRANOLOL HYDROCHLORIDE
62 4RANITIDINE HYDROCHLORIDE
63 1RISPERIDONE
64 1SODIUM POLYSTYRENE SULFONATE
65 2SULFAMETHOXAZOLE; TRIMETHOPRIM
66 2THEOPHYLLINE
67 2THIORIDAZINE HYDROCHLORIDE
68 2TRIAMCINOLONE ACETONIDE
69 1TRIHEXYPHENIDYL HYDROCHLORIDE
70 1TRIPROLIDINE HYDROCHLORIDE
71 1VALPROIC ACID
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01 55PAI HOLDINGS PHARM
02 68PHARM ASSOC
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01 9CONCENTRATE;ORAL
02 4CREAM;TOPICAL
03 5ELIXIR;ORAL
04 1GEL;TOPICAL
05 24INJECTABLE;INJECTION
06 1INJECTABLE;INTRAMUSCULAR, INTRAVENOUS
07 3LOTION;TOPICAL
08 6OINTMENT;TOPICAL
09 1POWDER;ORAL, RECTAL
10 1SOLUTION, ELIXIR;ORAL
11 1SOLUTION;DENTAL
12 34SOLUTION;ORAL
13 1SOLUTION;ORAL, RECTAL
14 5SOLUTION;TOPICAL
15 6SUSPENSION;ORAL
16 1SYRUP; ORAL
17 20SYRUP;ORAL
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01 10.01%
02 60.05%
03 20.1%
04 10.12%
05 10.25%
06 30.5%
07 11.25MG/5ML
08 11.5%
09 1100,000 UNITS/GM;0.1%
10 1100,000 UNITS/ML
11 4100MG/5ML
12 4100MG/ML
13 210GM/15ML
14 210MG/5ML
15 210MG/5ML;6.25MG/5ML
16 110MG/ML ***Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
17 210MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
18 112.5MG/5ML
19 1125MG/5ML
20 215MG/5ML
21 116MG/5ML
22 11GM/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
23 11MG/0.5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
24 21MG/ML
25 22%
26 12.5%;2.5%
27 12.5MG/5ML
28 2200MG/5ML;40MG/5ML
29 120MEQ/15ML
30 120MG/5ML
31 3250MG/5ML
32 12GM/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
33 52MG/5ML
34 12MG/5ML;10MG/5ML;30MG/5ML
35 12MG/ML
36 230MG/ML
37 130MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
38 1325MG/15ML;10MG/15ML
39 1325MG/15ML;7.5MG/15ML
40 14%
41 140MEQ/15ML
42 140MG/5ML
43 1453.6GM/BOT
44 1500MG/15ML;7.5MG/15ML
45 1500MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
46 150MG/5ML
47 85MG/5ML
48 15MG/ML
49 26.25MG/5ML
50 16GM/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
51 280MG/15ML
52 1EQ 1% BASE
53 1EQ 1.5GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
54 1EQ 10GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
55 3EQ 10MG BASE/5ML
56 2EQ 10MG BASE/ML
57 1EQ 15MG BASE/5ML
58 2EQ 15MG BASE/ML
59 1EQ 1GM BASE/VIAL
60 1EQ 1MG BASE/ML
61 2EQ 20MG BASE/5ML
62 2EQ 20MG BASE/ML
63 1EQ 25MG BASE/ML
64 1EQ 2GM BASE/VIAL
65 2EQ 2MG BASE/ML
66 3EQ 300MG BASE/5ML
67 1EQ 300MG CARBONATE/5ML
68 1EQ 30MG BASE/5ML
69 1EQ 30MG BASE/ML
70 2EQ 40MG BASE/ML
71 1EQ 4MG BASE/5ML
72 1EQ 50MG BASE/100ML
73 1EQ 5MG BASE/5ML
74 1EQ 7.5GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
75 1EQ 750MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
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01 123USA
Regulatory Info : DISCN
Registration Country : USA
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : SOLUTION;ORAL
Brand Name : HYDROCODONE BITARTRATE AN...
Dosage Strength : 500MG/15ML;7.5MG/15ML
Packaging :
Approval Date : 1998-03-13
Application Number : 40182
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : SOLUTION;ORAL
Brand Name : HYDROCODONE BITARTRATE AN...
Dosage Strength : 325MG/15ML;10MG/15ML
Packaging :
Approval Date : 2008-04-18
Application Number : 40834
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : SOLUTION;ORAL
Brand Name : HYDROCODONE BITARTRATE AN...
Dosage Strength : 325MG/15ML;7.5MG/15ML
Packaging :
Approval Date : 2013-05-10
Application Number : 40838
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SYRUP;ORAL
Brand Name : AMANTADINE HYDROCHLORIDE
Dosage Strength : 50MG/5ML
Packaging :
Approval Date : 1995-07-17
Application Number : 74509
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : ELIXIR;ORAL
Brand Name : BROMPHENIRAMINE MALEATE
Dosage Strength : 2MG/5ML
Packaging :
Approval Date : 1982-01-01
Application Number : 87517
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
BROMPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
Dosage Form : SYRUP;ORAL
Brand Name : BROMPHENIRAMINE MALEATE, ...
Dosage Strength : 2MG/5ML;10MG/5ML;30MG/...
Packaging :
Approval Date : 2014-07-21
Application Number : 202940
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : CEFOTAN
Dosage Strength : EQ 2GM BASE/VIAL
Packaging :
Approval Date : 1985-12-27
Application Number : 50588
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : CEFOTAN
Dosage Strength : EQ 10GM BASE/VIAL **Fe...
Packaging :
Approval Date : 1988-04-25
Application Number : 50588
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : CEFOTAN IN PLASTIC CONTAI...
Dosage Strength : EQ 40MG BASE/ML
Packaging :
Approval Date : 1993-07-30
Application Number : 50694
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : CEFOTAN IN PLASTIC CONTAI...
Dosage Strength : EQ 20MG BASE/ML
Packaging :
Approval Date : 1993-07-30
Application Number : 50694
Regulatory Info : DISCN
Registration Country : USA