01 1ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE
02 5ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
03 1ACRIVASTINE; PSEUDOEPHEDRINE HYDROCHLORIDE
04 7ALPROSTADIL
05 1ASPIRIN; OXYCODONE HYDROCHLORIDE
06 2ASPIRIN; OXYCODONE HYDROCHLORIDE; OXYCODONE TEREPHTHALATE
07 1Acetylsalicylic Acid; Dipyridamole
08 2BETHANECHOL CHLORIDE
09 10CENOBAMATE
10 1CLINDAMYCIN PHOSPHATE
11 2CLIOQUINOL
12 2CYANOCOBALAMIN
13 1CYPROTERONE ACETATE
14 1DALBAVANCIN (DALBAVANCIN HYDROCHLORIDE)
15 6DANTROLENE SODIUM
16 3DEXTROAMPHETAMINE SULFATE
17 1DICLOFENAC SODIUM
18 1DIPHENHYDRAMINE HYDROCHLORIDE
19 2DOXEPIN (DOXEPIN HYDROCHLORIDE)
20 1ETHINYL ESTRADIOL
21 1FLUDROCORTISONE 21-ACETATE
22 2FLUMETHASONE PIVALATE
23 1FOMEPIZOLE
24 1FOSFOMYCIN (FOSFOMYCIN TROMETHAMINE)
25 2FROVATRIPTAN (FROVATRIPTAN SUCCINATE)
26 1FROVATRIPTAN SUCCINATE
27 2HISTRELIN ACETATE
28 1ISOSORBIDE DINITRATE
29 2LABETALOL HYDROCHLORIDE
30 1MEGESTROL ACETATE
31 8METHADONE HYDROCHLORIDE
32 1METHIMAZOLE
33 2METHOCARBAMOL
34 2METHOXYFLURANE
35 2MORPHINE SULFATE
36 3NITROGLYCERIN
37 7OXYMORPHONE HYDROCHLORIDE
38 2PENBUTOLOL SULFATE
39 2PITOLISANT HYDROCHLORIDE
40 1PIZOTIFEN (PIZOTIFEN MALATE)
41 1PROPYLTHIOURACIL
42 1SINECATECHINS
43 2SUMATRIPTAN SUCCINATE
44 3TACROLIMUS
45 8TAPENTADOL (TAPENTADOL HYDROCHLORIDE)
46 4TESTOSTERONE
47 1TESTOSTERONE UNDECANOATE
48 4THEOPHYLLINE
49 3TRAMADOL HYDROCHLORIDE
50 1Testosteron
51 1Testosterone
52 1VALRUBICIN
53 3Zonisamide
01 2BOCA PHARMA LLC
02 50ENDO OPERATIONS
03 70ENDO OPERATIONS LTD.
04 5Endo Ventures Limited
05 1Endo Ventures Unlimited Company
01 1CAPSULE
02 2CAPSULE (SUSTAINED-RELEASE)
03 5CAPSULE, EXTENDED RELEASE;ORAL
04 4CAPSULE;ORAL
05 2CREAM
06 1Capsule For Inhalation
07 2DROPS
08 1GEL
09 1GEL, METERED;NASAL
10 1GEL, METERED;TRANSDERMAL
11 1GEL;TRANSDERMAL
12 3Hard Capsule
13 2IMPLANT;SUBCUTANEOUS
14 8INJECTABLE;INJECTION
15 1INJECTABLE;INTRAMUSCULAR
16 2INJECTABLE;SUBCUTANEOUS
17 1KIT
18 1LIQUID
19 1OINTMENT
20 3PATCH
21 1PELLET;IMPLANTATION
22 3POWDER FOR SOLUTION
23 6SOLUTION
24 1SOLUTION;INTRAVESICAL
25 1SOLUTION;TOPICAL
26 1SPRAY, METERED;NASAL
27 1SUSPENSION;ORAL
28 33TABLET
29 11TABLET (EXTENDED-RELEASE)
30 3TABLET (IMMEDIATE RELEASE)
31 7TABLET, EXTENDED RELEASE;ORAL
32 15TABLET;ORAL
33 2Transdermal Gel
01 10.005MG/VIAL
02 20.01MG/VIAL
03 10.02%/W/V
04 10.02%/W/W
05 20.02MG/VIAL
06 10.035MG
07 20.04MG/VIAL
08 10.1MG
09 10.2MG/HOUR
10 10.4MG/HOUR
11 10.5MG/INH
12 10.5MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
13 10.6MG/HOUR
14 10.75MG
15 11%
16 11%/W/V
17 11.5%/W/W
18 110%/W/W
19 9100MG
20 510MG
21 210MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
22 110MG/0.5GM ACTUATION **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
23 210MG/ML
24 212.5MG
25 1125MG/ML
26 2150MG
27 115MG
28 115MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
29 11G/ML
30 31MG
31 21MG/ML
32 22.5MG
33 5200MG
34 1200mg;25mg
35 120MG
36 220MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
37 220MG/VIAL
38 1250MG
39 725MG
40 12MG
41 13%/W/W
42 2300MG
43 130MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
44 1325MG;10MG
45 1325MG;2.25MG;0.19MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
46 1325MG;2.5MG
47 1325MG;4.5MG;0.38MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
48 1325MG;4.8355MG
49 1325MG;5MG
50 1325MG;5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
51 1325MG;7.5MG
52 13G/SACHET
53 13MG
54 1400MG
55 140MG
56 140MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
57 140MG/ML
58 14MG
59 1500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
60 1500MG/VIAL
61 1150MG
62 150MG/5GM PACKET
63 150mg
64 45MG
65 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
66 16MG
67 17.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
68 1712.8MG;60MG;32MG
69 1750MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
70 1750MG/3ML (250MG/ML)
71 275MG
72 18MG;60MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
73 299.9%
74 1EQ 1% BASE
75 1EQ 2.5MG BASE
76 1EQ 4MG BASE/0.5ML (EQ 8MG BASE/ML)
77 1EQ 6MG BASE/0.5ML (EQ 12MG BASE/ML)
01 70Canada
02 3Malta
03 1Spain
04 2Sweden
05 52USA
Regulatory Info : DISCN
Registration Country : USA
ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE
Dosage Form : TABLET;ORAL
Brand Name : ACETAMINOPHEN, CAFFEINE, ...
Dosage Strength : 712.8MG;60MG;32MG
Packaging :
Approval Date : 2007-04-03
Application Number : 40701
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Brand Name : PERCOCET
Dosage Strength : 325MG;2.5MG
Packaging :
Approval Date : 1999-06-25
Application Number : 40330
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Brand Name : PERCOCET
Dosage Strength : 325MG;5MG
Packaging :
Approval Date : 1999-06-25
Application Number : 40330
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Brand Name : PERCOCET
Dosage Strength : 325MG;7.5MG
Packaging :
Approval Date : 2001-11-23
Application Number : 40330
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Brand Name : PERCOCET
Dosage Strength : 325MG;10MG
Packaging :
Approval Date : 2001-11-23
Application Number : 40330
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Brand Name : PERCOCET
Dosage Strength : 325MG;5MG **Federal Re...
Packaging :
Approval Date : 1982-01-01
Application Number : 85106
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : Deregistered
Registration Country : Sweden
Acetylsalicylic Acid; Dipyridamole
Dosage Form : Capsule For Inhalation
Brand Name : Atranipar
Dosage Strength : 200mg;25mg
Packaging :
Approval Date : 2017-09-22
Application Number : 20150417000019
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : DISCN
Registration Country : USA
ACRIVASTINE; PSEUDOEPHEDRINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Brand Name : SEMPREX-D
Dosage Strength : 8MG;60MG **Federal Reg...
Packaging :
Approval Date : 1994-03-25
Application Number : 19806
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : EDEX
Dosage Strength : 0.005MG/VIAL
Packaging :
Approval Date : 1997-06-12
Application Number : 20649
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : EDEX
Dosage Strength : 0.01MG/VIAL
Packaging :
Approval Date : 1997-06-12
Application Number : 20649
Regulatory Info : RX
Registration Country : USA
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