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 4DANTROLENE SODIUM
10 1FROVATRIPTAN SUCCINATE
11 2HISTRELIN ACETATE
12 1ISOSORBIDE DINITRATE
13 1MEGESTROL ACETATE
14 2METHOCARBAMOL
15 7OXYMORPHONE HYDROCHLORIDE
16 2PENBUTOLOL SULFATE
17 1PROPYLTHIOURACIL
18 2SUMATRIPTAN SUCCINATE
19 3TESTOSTERONE
20 1TESTOSTERONE UNDECANOATE
21 4THEOPHYLLINE
22 1VALRUBICIN
01 5CAPSULE, EXTENDED RELEASE;ORAL
02 4CAPSULE;ORAL
03 1GEL, METERED;NASAL
04 1GEL, METERED;TRANSDERMAL
05 1GEL;TRANSDERMAL
06 2IMPLANT;SUBCUTANEOUS
07 8INJECTABLE;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06 10.5MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 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08 210MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
09 110MG/0.5GM ACTUATION **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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11 115MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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13 220MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
14 120MG/VIAL
15 125MG
16 1300MG
17 130MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
18 1325MG;10MG
19 1325MG;2.25MG;0.19MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
20 1325MG;2.5MG
21 1325MG;4.5MG;0.38MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
22 1325MG;4.8355MG
23 1325MG;5MG
24 1325MG;5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
25 1325MG;7.5MG
26 1400MG
27 140MG
28 140MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
29 140MG/ML
30 1500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
31 450MG
32 150MG/5GM PACKET
33 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
34 17.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
35 1712.8MG;60MG;32MG
36 1750MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
37 1750MG/3ML (250MG/ML)
38 175MG
39 18MG;60MG
40 1EQ 1% BASE
41 1EQ 2.5MG BASE
42 1EQ 4MG BASE/0.5ML (EQ 8MG BASE/ML)
43 1EQ 6MG BASE/0.5ML (EQ 12MG BASE/ML)
01 26DISCN
02 26RX
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
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
