01 3ACETAMINOPHEN; CODEINE PHOSPHATE
02 6ACETAMINOPHEN; HYDROCODONE BITARTRATE
03 3ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
04 13AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE
05 2AMPHETAMINE SULFATE
06 1BROMPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
07 2BUPRENORPHINE HYDROCHLORIDE
08 2BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
09 3DEXMETHYLPHENIDATE HYDROCHLORIDE
10 5FENOFIBRATE
11 8HYDROMORPHONE HYDROCHLORIDE
12 3LEVOBUPIVACAINE HYDROCHLORIDE
13 7LISDEXAMFETAMINE DIMESYLATE
14 1MACITENTAN
15 2MARAVIROC
16 11METHYLPHENIDATE HYDROCHLORIDE
17 8MORPHINE SULFATE
18 3NALOXONE HYDROCHLORIDE; OXYCODONE HYDROCHLORIDE
19 6OXYCODONE HYDROCHLORIDE
20 1SCOPOLAMINE
21 1SULFAPHENAZOLE
22 2TAPENTADOL HYDROCHLORIDE
23 3THEOPHYLLINE
24 3TRAMADOL HYDROCHLORIDE
25 2VARENICLINE TARTRATE
26 2ZOLPIDEM TARTRATE
01 17CAPSULE, EXTENDED RELEASE;ORAL
02 10CAPSULE;ORAL
03 3INJECTABLE;INJECTION
04 5SOLUTION;ORAL
05 1SYRUP;ORAL
06 1SYSTEM;TRANSDERMAL
07 18TABLET, EXTENDED RELEASE;ORAL
08 42TABLET;ORAL
09 6TABLET;SUBLINGUAL
01 21.25MG;1.25MG;1.25MG;1.25MG
02 11.75MG
03 11.875MG;1.875MG;1.875MG;1.875MG
04 2100MG
05 1100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
06 2100MG/5ML
07 610MG
08 110MG/5ML
09 110MG;20MG
10 112MG
11 1134MG
12 1150MG
13 315MG
14 1160MG
15 116MG
16 118MG
17 11MG/72HR
18 12.5MG
19 22.5MG;2.5MG;2.5MG;2.5MG
20 2200MG
21 1200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
22 320MG
23 120MG/5ML
24 120MG;40MG
25 124MG
26 127MG
27 12MG
28 12MG/5ML;10MG/5ML;30MG/5ML
29 13.125MG;3.125MG;3.125MG;3.125MG
30 13.5MG
31 23.75MG;3.75MG;3.75MG;3.75MG
32 2300MG
33 1300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
34 1300MG;10MG
35 1300MG;15MG
36 1300MG;30MG
37 1300MG;5MG
38 1300MG;60MG
39 1300MG;7.5MG
40 430MG
41 2325MG;10MG
42 2325MG;5MG
43 2325MG;7.5MG
44 132MG
45 136MG
46 1400MG
47 240MG
48 14MG
49 1500MG
50 250MG
51 254MG
52 35MG
53 15MG/5ML
54 15MG;10MG
55 25MG;5MG;5MG;5MG
56 16.25MG;6.25MG;6.25MG;6.25MG
57 1600MG
58 360MG
59 167MG
60 27.5MG;7.5MG;7.5MG;7.5MG
61 170MG
62 175MG
63 18MG
64 1EQ 0.5MG BASE
65 1EQ 1MG BASE
66 1EQ 2.5MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
67 1EQ 2MG BASE
68 1EQ 2MG BASE;EQ 0.5MG BASE
69 1EQ 5MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
70 1EQ 7.5MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
71 1EQ 8MG BASE
72 1EQ 8MG BASE;EQ 2MG BASE
01 42DISCN
02 58RX
03 3Blank
RLD : No
TE Code :
ACETAMINOPHEN; CODEINE PHOSPHATE
Dosage Form : TABLET; ORAL
Proprietary Name : ACETAMINOPHEN AND CODEIN...
Dosage Strength : 300MG;60MG
Approval Date : 1988-02-10
Application Number : 89673
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; CODEINE PHOSPHATE
Dosage Form : TABLET; ORAL
Proprietary Name : ACETAMINOPHEN AND CODEIN...
Dosage Strength : 300MG;15MG
Approval Date : 1988-02-10
Application Number : 89673
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; CODEINE PHOSPHATE
Dosage Form : TABLET; ORAL
Proprietary Name : ACETAMINOPHEN AND CODEIN...
Dosage Strength : 300MG;30MG
Approval Date : 1988-02-10
Application Number : 89673
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code : AA
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET; ORAL
Proprietary Name : HYDROCODONE BITARTRATE A...
Dosage Strength : 325MG;5MG
Approval Date : 2016-04-12
Application Number : 202991
RX/OTC/DISCN : RX
RLD : No
TE Code : AA
RLD : No
TE Code : AA
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET; ORAL
Proprietary Name : HYDROCODONE BITARTRATE A...
Dosage Strength : 325MG;7.5MG
Approval Date : 2016-04-12
Application Number : 202991
RX/OTC/DISCN : RX
RLD : No
TE Code : AA
RLD : No
TE Code : AA
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET; ORAL
Proprietary Name : HYDROCODONE BITARTRATE A...
Dosage Strength : 325MG;10MG
Approval Date : 2016-04-12
Application Number : 202991
RX/OTC/DISCN : RX
RLD : No
TE Code : AA
RLD : No
TE Code :
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET; ORAL
Proprietary Name : HYDROCODONE BITARTRATE A...
Dosage Strength : 300MG;5MG
Approval Date : 2018-03-30
Application Number : 207808
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 : 300MG;7.5MG
Approval Date : 2018-03-30
Application Number : 207808
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 : 300MG;10MG
Approval Date : 2018-03-30
Application Number : 207808
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code : AA
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Dosage Form : TABLET; ORAL
Proprietary Name : OXYCODONE AND ACETAMINOP...
Dosage Strength : 325MG;5MG
Approval Date : 2014-08-28
Application Number : 201278
RX/OTC/DISCN : RX
RLD : No
TE Code : AA
Purdue Pharmaceuticals L.p is a supplier offers 2 products (APIs, Excipients or Intermediates).
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