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 4DANTROLENE SODIUM
11 1FROVATRIPTAN SUCCINATE
12 2HISTRELIN ACETATE
13 1ISOSORBIDE DINITRATE
14 1MEGESTROL ACETATE
15 2METHOCARBAMOL
16 7OXYMORPHONE HYDROCHLORIDE
17 2PENBUTOLOL SULFATE
18 1PROPYLTHIOURACIL
19 2SUMATRIPTAN SUCCINATE
20 3TESTOSTERONE
21 1TESTOSTERONE UNDECANOATE
22 4THEOPHYLLINE
23 1Testosteron
24 1Testosterone
25 1VALRUBICIN
01 2BOCA PHARMA LLC
02 50ENDO OPERATIONS
03 2Endo Ventures Limited
04 1Endo Ventures Unlimited Company
01 5CAPSULE, EXTENDED RELEASE;ORAL
02 4CAPSULE;ORAL
03 1Capsule For Inhalation
04 1GEL, METERED;NASAL
05 1GEL, METERED;TRANSDERMAL
06 1GEL;TRANSDERMAL
07 2IMPLANT;SUBCUTANEOUS
08 8INJECTABLE;INJECTION
09 1INJECTABLE;INTRAMUSCULAR
10 2INJECTABLE;SUBCUTANEOUS
11 1PELLET;IMPLANTATION
12 1SOLUTION;INTRAVESICAL
13 1SOLUTION;TOPICAL
14 1SPRAY, METERED;NASAL
15 1SUSPENSION;ORAL
16 7TABLET, EXTENDED RELEASE;ORAL
17 15TABLET;ORAL
18 2Transdermal Gel
01 10.005MG/VIAL
02 20.01MG/VIAL
03 20.02MG/VIAL
04 20.04MG/VIAL
05 10.5MG/INH
06 10.5MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
07 2100MG
08 210MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
09 110MG/0.5GM ACTUATION **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
10 1125MG/ML
11 115MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
12 1200MG
13 1200mg;25mg
14 220MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
15 120MG/VIAL
16 125MG
17 1300MG
18 130MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
19 1325MG;10MG
20 1325MG;2.25MG;0.19MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
21 1325MG;2.5MG
22 1325MG;4.5MG;0.38MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
23 1325MG;4.8355MG
24 1325MG;5MG
25 1325MG;5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
26 1325MG;7.5MG
27 1400MG
28 140MG
29 140MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
30 140MG/ML
31 1500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
32 550MG
33 150MG/5GM PACKET
34 150mg
35 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
36 17.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
37 1712.8MG;60MG;32MG
38 1750MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
39 1750MG/3ML (250MG/ML)
40 175MG
41 18MG;60MG
42 1EQ 1% BASE
43 1EQ 2.5MG BASE
44 1EQ 4MG BASE/0.5ML (EQ 8MG BASE/ML)
45 1EQ 6MG BASE/0.5ML (EQ 12MG BASE/ML)
01 1Spain
02 2Sweden
03 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
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
