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 2FAMOTIDINE
20 1FENFLURAMINE HYDROCHLORIDE
21 1GLUTETHIMIDE
22 3HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE
23 6LACOSAMIDE
24 8LEVETIRACETAM
25 1MIDAZOLAM
26 2MOEXIPRIL HYDROCHLORIDE
27 2PHENTERMINE RESIN COMPLEX
28 1PREDNISONE
29 1PSEUDOEPHEDRINE POLISTIREX
30 6ROTIGOTINE
31 1ROZANOLIXIZUMAB-NOLI
32 4THEOPHYLLINE
33 3ZILUCOPLAN SODIUM
01 1AEROSOL, METERED;INHALATION
02 1AEROSOL;NASAL
03 10CAPSULE, EXTENDED RELEASE;ORAL
04 1CAPSULE;ORAL
05 6FILM, EXTENDED RELEASE;TRANSDERMAL
06 1INJECTABLE; INJECTION
07 1INJECTABLE;INJECTION
08 1INJECTABLE;INTRAVENOUS
09 1INJECTABLE;SUBCUTANEOUS
10 2SOLUTION;INTRAVENOUS
11 4SOLUTION;ORAL
12 3SOLUTION;SUBCUTANEOUS
13 1SPRAY;NASAL
14 3SUSPENSION, EXTENDED RELEASE;ORAL
15 2TABLET, EXTENDED RELEASE;ORAL
16 11TABLET, ORALLY DISINTEGRATING;ORAL
17 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01 10.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
02 10.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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06 110MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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08 110MG;100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
09 112.5MG;15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
10 112.5MG;7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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14 115MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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17 11MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 12MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
31 12MG/24HR
32 13MG/24HR
33 140MG
34 14MG/24HR
35 3500MG
36 1500MG/5ML (100MG/ML)
37 2500MG;10MG
38 2500MG;5MG
39 1500MG;5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
40 450MG
41 150MG/5ML (10MG/ML)
42 15MG
43 15MG/SPRAY
44 1650MG;7.5MG
45 16MG/24HR
46 17.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
47 2750MG
48 275MG
49 18MG/24HR
50 2EQ 0.1MG PHOSPHATE/INH
51 1EQ 10MG BASE;EQ 10MG BASE
52 1EQ 15MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
53 1EQ 16.6MG BASE/0.416ML (EQ 16.6MG BASE/0.416ML)
54 1EQ 2.2MG BASE/ML
55 1EQ 23MG BASE/0.574ML (EQ 23MG BASE/0.574ML)
56 1EQ 2MG BASE
57 1EQ 3.75MG BASE;EQ 3.75MG BASE
58 1EQ 30MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
59 1EQ 32.4MG BASE/0.81ML (EQ 32.4 BASE/0.81ML)
60 1EQ 4MG BASE
61 1EQ 4MG MALEATE/5ML;EQ 37.5MG HCL/5ML
62 1EQ 6.25MG BASE;EQ 6.25MG BASE
63 1EQ 60MG HYDROCHLORIDE/5ML
64 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 32RX
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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