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 1CLINDAMYCIN PHOSPHATE
08 2CYANOCOBALAMIN
09 1FROVATRIPTAN SUCCINATE
10 2HISTRELIN ACETATE
11 1ISOSORBIDE DINITRATE
12 1MEGESTROL ACETATE
13 2METHOCARBAMOL
14 7OXYMORPHONE HYDROCHLORIDE
15 2PENBUTOLOL SULFATE
16 1PROPYLTHIOURACIL
17 2SUMATRIPTAN SUCCINATE
18 3TESTOSTERONE
19 1TESTOSTERONE UNDECANOATE
20 4THEOPHYLLINE
21 1VALRUBICIN
01 5CAPSULE, EXTENDED RELEASE;ORAL
02 1CAPSULE;ORAL
03 1GEL, METERED;NASAL
04 1GEL, METERED;TRANSDERMAL
05 1GEL;TRANSDERMAL
06 2IMPLANT;SUBCUTANEOUS
07 7INJECTABLE;INJECTION
08 1INJECTABLE;INTRAMUSCULAR
09 2INJECTABLE;SUBCUTANEOUS
10 1PELLET;IMPLANTATION
11 1SOLUTION;INTRAVESICAL
12 1SOLUTION;TOPICAL
13 1SPRAY, METERED;NASAL
14 1SUSPENSION;ORAL
15 7TABLET, EXTENDED RELEASE;ORAL
16 15TABLET;ORAL
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06 10.5MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 1100MG
08 210MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
09 110MG/0.5GM ACTUATION **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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11 115MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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13 220MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
14 1300MG
15 130MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
16 1325MG;10MG
17 1325MG;2.25MG;0.19MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
18 1325MG;2.5MG
19 1325MG;4.5MG;0.38MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
20 1325MG;4.8355MG
21 1325MG;5MG
22 1325MG;5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
23 1325MG;7.5MG
24 1400MG
25 140MG
26 140MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
27 140MG/ML
28 1500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
29 350MG
30 150MG/5GM PACKET
31 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
32 17.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
33 1712.8MG;60MG;32MG
34 1750MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
35 1750MG/3ML (250MG/ML)
36 175MG
37 18MG;60MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
38 1EQ 1% BASE
39 1EQ 2.5MG BASE
40 1EQ 4MG BASE/0.5ML (EQ 8MG BASE/ML)
41 1EQ 6MG BASE/0.5ML (EQ 12MG BASE/ML)
01 26DISCN
02 22RX
RLD : No
TE Code :
ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE
Dosage Form : TABLET; ORAL
Proprietary Name : ACETAMINOPHEN, CAFFEINE,...
Dosage Strength : 712.8MG;60MG;32MG
Approval Date : 2007-04-03
Application Number : 40701
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code : AA
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Dosage Form : TABLET; ORAL
Proprietary Name : PERCOCET
Dosage Strength : 325MG;2.5MG
Approval Date : 1999-06-25
Application Number : 40330
RX/OTC/DISCN : RX
RLD : No
TE Code : AA
RLD : No
TE Code : AA
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Dosage Form : TABLET; ORAL
Proprietary Name : PERCOCET
Dosage Strength : 325MG;5MG
Approval Date : 1999-06-25
Application Number : 40330
RX/OTC/DISCN : RX
RLD : No
TE Code : AA
RLD : No
TE Code : AA
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Dosage Form : TABLET; ORAL
Proprietary Name : PERCOCET
Dosage Strength : 325MG;7.5MG
Approval Date : 2001-11-23
Application Number : 40330
RX/OTC/DISCN : RX
RLD : No
TE Code : AA
RLD : No
TE Code : AA
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Dosage Form : TABLET; ORAL
Proprietary Name : PERCOCET
Dosage Strength : 325MG;10MG
Approval Date : 2001-11-23
Application Number : 40330
RX/OTC/DISCN : RX
RLD : No
TE Code : AA
RLD : Yes
TE Code :
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Dosage Form : TABLET; ORAL
Proprietary Name : PERCOCET
Dosage Strength : 325MG;5MG **Federal Regi...
Approval Date : 1982-01-01
Application Number : 85106
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
ACRIVASTINE; PSEUDOEPHEDRINE HYDROCHLORIDE
Dosage Form : CAPSULE; ORAL
Proprietary Name : SEMPREX-D
Dosage Strength : 8MG;60MG **Federal Regis...
Approval Date : 1994-03-25
Application Number : 19806
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : EDEX
Dosage Strength : 0.005MG/VIAL
Approval Date : 1997-06-12
Application Number : 20649
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code : AP
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : EDEX
Dosage Strength : 0.01MG/VIAL
Approval Date : 1997-06-12
Application Number : 20649
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AP
RLD : Yes
TE Code : AP
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : EDEX
Dosage Strength : 0.02MG/VIAL
Approval Date : 1997-06-12
Application Number : 20649
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AP
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Find a price of Glycopyrronium Bromide bulk offered by Endo International
