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07 10.5MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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12 210MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
13 110MG/0.5GM ACTUATION **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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17 115MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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25 220MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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29 130MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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