01 1ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE
02 1ACRIVASTINE; PSEUDOEPHEDRINE HYDROCHLORIDE
03 7ALPROSTADIL
04 1ASPIRIN; OXYCODONE HYDROCHLORIDE
05 2ASPIRIN; OXYCODONE HYDROCHLORIDE; OXYCODONE TEREPHTHALATE
06 1CLINDAMYCIN PHOSPHATE
07 2CYANOCOBALAMIN
08 1FROVATRIPTAN SUCCINATE
09 2HISTRELIN ACETATE
10 1ISOSORBIDE DINITRATE
11 1MEGESTROL ACETATE
12 2METHOCARBAMOL
13 7OXYMORPHONE HYDROCHLORIDE
14 2PENBUTOLOL SULFATE
15 2SUMATRIPTAN SUCCINATE
16 3TESTOSTERONE
17 1TESTOSTERONE UNDECANOATE
18 4THEOPHYLLINE
19 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 9TABLET;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06 10.5MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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08 210MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
09 110MG/0.5GM ACTUATION **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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11 115MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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13 220MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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15 130MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
16 1325MG;2.25MG;0.19MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
17 1325MG;4.5MG;0.38MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
18 1325MG;4.8355MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
19 1400MG
20 140MG
21 140MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
22 140MG/ML
23 1500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
24 250MG
25 150MG/5GM PACKET
26 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
27 17.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
28 1712.8MG;60MG;32MG
29 1750MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
30 1750MG/3ML (250MG/ML)
31 175MG
32 18MG;60MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
33 1EQ 1% BASE
34 1EQ 2.5MG BASE
35 1EQ 4MG BASE/0.5ML (EQ 8MG BASE/ML)
36 1EQ 6MG BASE/0.5ML (EQ 12MG BASE/ML)
01 27DISCN
02 15RX
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 : 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
RLD : Yes
TE Code : AP
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : EDEX
Dosage Strength : 0.04MG/VIAL
Approval Date : 1997-06-12
Application Number : 20649
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AP
RLD : Yes
TE Code :
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : EDEX
Dosage Strength : 0.01MG/VIAL
Approval Date : 1998-07-30
Application Number : 20649
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : EDEX
Dosage Strength : 0.02MG/VIAL
Approval Date : 1998-07-30
Application Number : 20649
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : EDEX
Dosage Strength : 0.04MG/VIAL
Approval Date : 1998-07-30
Application Number : 20649
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
ASPIRIN; OXYCODONE HYDROCHLORIDE
Dosage Form : TABLET; ORAL
Proprietary Name : PERCODAN
Dosage Strength : 325MG;4.8355MG **Federal...
Approval Date : 2005-08-05
Application Number : 7337
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
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Find Glycopyrronium Bromide bulk offered by Endo International
