01 5ACETAMINOPHEN; HYDROCODONE BITARTRATE
02 2ALBUTEROL SULFATE
03 4ALPRAZOLAM
04 6AMITRIPTYLINE HYDROCHLORIDE
05 3AMPHETAMINE RESIN COMPLEX; DEXTROAMPHETAMINE RESIN COMPLEX
06 1ASPIRIN; HYDROCODONE BITARTRATE
07 2BACLOFEN
08 1BICALUTAMIDE
09 1BIMEKIZUMAB-BKZX
10 7BRIVARACETAM
11 3CARBIDOPA; LEVODOPA
12 1CERTOLIZUMAB PEGOL
13 1CHLORPHENIRAMINE MALEATE; PSEUDOEPHEDRINE HYDROCHLORIDE
14 1CHLORPHENIRAMINE POLISTIREX; HYDROCODONE POLISTIREX
15 1CHLORPHENIRAMINE POLISTIREX; PHENYLPROPANOLAMINE POLISTIREX
16 1CROMOLYN SODIUM
17 2DEXAMETHASONE SODIUM PHOSPHATE
18 1DIETHYLPROPION HYDROCHLORIDE
19 1DOXECITINE; DOXRIBTIMINE
20 2FAMOTIDINE
21 1FENFLURAMINE HYDROCHLORIDE
22 1GLUTETHIMIDE
23 3HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE
24 6LACOSAMIDE
25 8LEVETIRACETAM
26 1MIDAZOLAM
27 2MOEXIPRIL HYDROCHLORIDE
28 2PHENTERMINE RESIN COMPLEX
29 1PREDNISONE
30 1PSEUDOEPHEDRINE POLISTIREX
31 6ROTIGOTINE
32 1ROZANOLIXIZUMAB-NOLI
33 4THEOPHYLLINE
34 3ZILUCOPLAN SODIUM
01 1AEROSOL, METERED;INHALATION
02 1AEROSOL;NASAL
03 10CAPSULE, EXTENDED RELEASE;ORAL
04 1CAPSULE;ORAL
05 6FILM, EXTENDED RELEASE;TRANSDERMAL
06 1FOR SOLUTION;ORAL
07 1INJECTABLE; INJECTION
08 1INJECTABLE;INJECTION
09 1INJECTABLE;INTRAVENOUS
10 1INJECTABLE;SUBCUTANEOUS
11 2SOLUTION;INTRAVENOUS
12 4SOLUTION;ORAL
13 3SOLUTION;SUBCUTANEOUS
14 1SPRAY;NASAL
15 3SUSPENSION, EXTENDED RELEASE;ORAL
16 2TABLET, EXTENDED RELEASE;ORAL
17 11TABLET, ORALLY DISINTEGRATING;ORAL
18 36TABLET;ORAL
01 10.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
02 10.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
03 4100MG
04 1100MG/ML
05 210MG
06 110MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
07 210MG/ML
08 110MG;100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
09 112.5MG;15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
10 112.5MG;7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
11 112MG;120MG
12 2130MG
13 2150MG
14 115MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
15 1160ML
16 11GM
17 11MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
18 11MG/24HR
19 2200MG
20 1200MG/20ML (10MG/ML)
21 120MG
22 120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
23 1250MG
24 325MG
25 125MG;100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
26 125MG;15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
27 125MG;250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
28 2260MG
29 1280MG/2ML(140MG/ML)
30 12GM/PACKET;2GM/PACKET
31 12MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
32 12MG/24HR
33 13MG/24HR
34 140MG
35 14MG/24HR
36 3500MG
37 1500MG/5ML (100MG/ML)
38 2500MG;10MG
39 2500MG;5MG
40 1500MG;5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
41 450MG
42 150MG/5ML (10MG/ML)
43 15MG
44 15MG/SPRAY
45 1650MG;7.5MG
46 16MG/24HR
47 17.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
48 2750MG
49 275MG
50 18MG/24HR
51 2EQ 0.1MG PHOSPHATE/INH
52 1EQ 10MG BASE;EQ 10MG BASE
53 1EQ 15MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
54 1EQ 16.6MG BASE/0.416ML (EQ 16.6MG BASE/0.416ML)
55 1EQ 2.2MG BASE/ML
56 1EQ 23MG BASE/0.574ML (EQ 23MG BASE/0.574ML)
57 1EQ 2MG BASE
58 1EQ 3.75MG BASE;EQ 3.75MG BASE
59 1EQ 30MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
60 1EQ 32.4MG BASE/0.81ML (EQ 32.4 BASE/0.81ML)
61 1EQ 4MG BASE
62 1EQ 4MG MALEATE/5ML;EQ 37.5MG HCL/5ML
63 1EQ 6.25MG BASE;EQ 6.25MG BASE
64 1EQ 60MG HYDROCHLORIDE/5ML
65 1EQ 8MG MALEATE/5ML;EQ 10MG BITARTRATE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
01 49DISCN
02 33RX
03 4Blank
RLD : No
TE Code :
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET; ORAL
Proprietary Name : LORTAB
Dosage Strength : 500MG;10MG
Approval Date : 1996-01-26
Application Number : 40100
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET; ORAL
Proprietary Name : HYDROCODONE BITARTRATE A...
Dosage Strength : 650MG;7.5MG
Approval Date : 1996-11-21
Application Number : 40134
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET; ORAL
Proprietary Name : HYDROCODONE BITARTRATE A...
Dosage Strength : 500MG;10MG
Approval Date : 1997-08-13
Application Number : 40210
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET; ORAL
Proprietary Name : LORTAB
Dosage Strength : 500MG;5MG
Approval Date : 1982-07-09
Application Number : 87722
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET; ORAL
Proprietary Name : CO-GESIC
Dosage Strength : 500MG;5MG
Approval Date : 1982-05-03
Application Number : 87757
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : ALBUTEROL SULFATE
Dosage Strength : EQ 2MG BASE
Approval Date : 1992-09-29
Application Number : 73120
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : ALBUTEROL SULFATE
Dosage Strength : EQ 4MG BASE
Approval Date : 1992-09-29
Application Number : 73121
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET, ORALLY DISINTEGRATING;...
Proprietary Name : NIRAVAM
Dosage Strength : 0.25MG **Federal Registe...
Approval Date : 2005-01-19
Application Number : 21726
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET, ORALLY DISINTEGRATING;...
Proprietary Name : NIRAVAM
Dosage Strength : 0.5MG **Federal Register...
Approval Date : 2005-01-19
Application Number : 21726
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET, ORALLY DISINTEGRATING;...
Proprietary Name : NIRAVAM
Dosage Strength : 1MG **Federal Register d...
Approval Date : 2005-01-19
Application Number : 21726
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
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