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 1CLINDAMYCIN PHOSPHATE
09 2CYANOCOBALAMIN
10 1CYPROTERONE ACETATE
11 1DALBAVANCIN (DALBAVANCIN HYDROCHLORIDE)
12 3DEXTROAMPHETAMINE SULFATE
13 1ETHINYL ESTRADIOL
14 1FLUDROCORTISONE 21-ACETATE
15 1FOMEPIZOLE
16 1FOSFOMYCIN (FOSFOMYCIN TROMETHAMINE)
17 2FROVATRIPTAN (FROVATRIPTAN SUCCINATE)
18 1FROVATRIPTAN SUCCINATE
19 2HISTRELIN ACETATE
20 1ISOSORBIDE DINITRATE
21 1MEGESTROL ACETATE
22 8METHADONE HYDROCHLORIDE
23 2METHOCARBAMOL
24 2METHOXYFLURANE
25 2MORPHINE SULFATE
26 3NITROGLYCERIN
27 7OXYMORPHONE HYDROCHLORIDE
28 2PENBUTOLOL SULFATE
29 2PITOLISANT HYDROCHLORIDE
30 1SINECATECHINS
31 2SUMATRIPTAN SUCCINATE
32 3TACROLIMUS
33 8TAPENTADOL (TAPENTADOL HYDROCHLORIDE)
34 3TESTOSTERONE
35 1TESTOSTERONE UNDECANOATE
36 4THEOPHYLLINE
37 3TRAMADOL HYDROCHLORIDE
38 1Testosteron
39 1Testosterone
40 1VALRUBICIN
41 3Zonisamide
01 2BOCA PHARMA LLC
02 45ENDO OPERATIONS
03 43ENDO OPERATIONS LTD.
04 5Endo Ventures Limited
05 1Endo Ventures Unlimited Company
01 2CAPSULE (SUSTAINED-RELEASE)
02 5CAPSULE, EXTENDED RELEASE;ORAL
03 1CAPSULE;ORAL
04 1Capsule For Inhalation
05 1GEL, METERED;NASAL
06 1GEL, METERED;TRANSDERMAL
07 1GEL;TRANSDERMAL
08 3Hard Capsule
09 2IMPLANT;SUBCUTANEOUS
10 7INJECTABLE;INJECTION
11 1INJECTABLE;INTRAMUSCULAR
12 2INJECTABLE;SUBCUTANEOUS
13 1KIT
14 1LIQUID
15 1OINTMENT
16 3PATCH
17 1PELLET;IMPLANTATION
18 2POWDER FOR SOLUTION
19 5SOLUTION
20 1SOLUTION;INTRAVESICAL
21 1SOLUTION;TOPICAL
22 1SPRAY, METERED;NASAL
23 1SUSPENSION;ORAL
24 14TABLET
25 11TABLET (EXTENDED-RELEASE)
26 3TABLET (IMMEDIATE RELEASE)
27 7TABLET, EXTENDED RELEASE;ORAL
28 14TABLET;ORAL
29 2Transdermal Gel
01 10.005MG/VIAL
02 20.01MG/VIAL
03 20.02MG/VIAL
04 10.035MG
05 20.04MG/VIAL
06 10.1MG
07 10.2MG/HOUR
08 10.4MG/HOUR
09 10.5MG/INH
10 10.5MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
11 10.6MG/HOUR
12 10.75MG
13 110%/W/W
14 5100MG
15 310MG
16 210MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
17 110MG/0.5GM ACTUATION **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
18 210MG/ML
19 1125MG/ML
20 1150MG
21 115MG
22 115MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
23 11G/ML
24 21MG
25 21MG/ML
26 22.5MG
27 3200MG
28 1200mg;25mg
29 120MG
30 220MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
31 1250MG
32 225MG
33 12MG
34 2300MG
35 130MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
36 1325MG;10MG
37 1325MG;2.25MG;0.19MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
38 1325MG;2.5MG
39 1325MG;4.5MG;0.38MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
40 1325MG;4.8355MG
41 1325MG;5MG
42 1325MG;5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
43 1325MG;7.5MG
44 13G/SACHET
45 1400MG
46 140MG
47 140MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
48 140MG/ML
49 14MG
50 1500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
51 1500MG/VIAL
52 650MG
53 150MG/5GM PACKET
54 150mg
55 45MG
56 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
57 17.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
58 1712.8MG;60MG;32MG
59 1750MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
60 1750MG/3ML (250MG/ML)
61 275MG
62 18MG;60MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
63 299.9%
64 1EQ 1% BASE
65 1EQ 2.5MG BASE
66 1EQ 4MG BASE/0.5ML (EQ 8MG BASE/ML)
67 1EQ 6MG BASE/0.5ML (EQ 12MG BASE/ML)
01 43Canada
02 3Malta
03 1Spain
04 2Sweden
05 47USA
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 : 22-09-2017
Application Number : 2.02E+13
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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Find a price of Glycopyrronium Bromide bulk offered by Endo International
