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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 5BUPRENORPHINE
08 2BUPRENORPHINE HYDROCHLORIDE
09 2BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
10 3DEXMETHYLPHENIDATE HYDROCHLORIDE
11 3DRONABINOL
12 5FENOFIBRATE
13 7HYDROCODONE BITARTRATE
14 8HYDROMORPHONE HYDROCHLORIDE
15 3LEVOBUPIVACAINE HYDROCHLORIDE
16 1LIDOCAINE; PRILOCAINE
17 7LISDEXAMFETAMINE DIMESYLATE
18 1MACITENTAN
19 17METHYLPHENIDATE HYDROCHLORIDE
20 13MORPHINE SULFATE
21 2NALMEFENE HYDROCHLORIDE
22 3NALOXONE HYDROCHLORIDE; OXYCODONE HYDROCHLORIDE
23 13OXYCODONE HYDROCHLORIDE
24 1SCOPOLAMINE
25 1SULFAPHENAZOLE
26 2TAPENTADOL HYDROCHLORIDE
27 3THEOPHYLLINE
28 3TRAMADOL HYDROCHLORIDE
29 2ZOLPIDEM TARTRATE
01 23CAPSULE, EXTENDED RELEASE;ORAL
02 13CAPSULE;ORAL
03 1CREAM;TOPICAL
04 5FILM, EXTENDED RELEASE;TRANSDERMAL
05 3INJECTABLE;INJECTION
06 1SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
07 1SOLUTION;INTRAMUSCULAR, SUBCUTANEOUS
08 5SOLUTION;ORAL
09 1SYRUP;ORAL
10 1SYSTEM;TRANSDERMAL
11 37TABLET, EXTENDED RELEASE;ORAL
12 38TABLET;ORAL
13 6TABLET;SUBLINGUAL
01 21.25MG;1.25MG;1.25MG;1.25MG
02 11.75MG
03 11.875MG;1.875MG;1.875MG;1.875MG
04 4100MG
05 1100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
06 2100MG/5ML
07 110MCG/HR
08 810MG
09 110MG/5ML
10 110MG;20MG
11 1120MG
12 112MG
13 1134MG
14 115MCG/HR
15 515MG
16 1160MG
17 116MG
18 118MG
19 11MG/72HR
20 12.5%;2.5%
21 22.5MG
22 22.5MG;2.5MG;2.5MG;2.5MG
23 3200MG
24 1200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
25 120MCG/HR
26 520MG
27 120MG/5ML
28 120MG;40MG
29 124MG
30 125MG
31 127MG
32 12MG
33 12MG/5ML;10MG/5ML;30MG/5ML
34 13.125MG;3.125MG;3.125MG;3.125MG
35 13.5MG
36 23.75MG;3.75MG;3.75MG;3.75MG
37 1300MG
38 1300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
39 1300MG;10MG
40 1300MG;15MG
41 1300MG;30MG
42 1300MG;5MG
43 1300MG;60MG
44 1300MG;7.5MG
45 730MG
46 2325MG;10MG
47 2325MG;5MG
48 2325MG;7.5MG
49 132MG
50 135MG
51 136MG
52 1400MG
53 440MG
54 145MG
55 14MG
56 1500MG
57 250MG
58 254MG
59 155MG
60 15MCG/HR
61 45MG
62 15MG/5ML
63 15MG;10MG
64 25MG;5MG;5MG;5MG
65 16.25MG;6.25MG;6.25MG;6.25MG
66 1600MG
67 660MG
68 167MG
69 17.5MCG/HR
70 27.5MG;7.5MG;7.5MG;7.5MG
71 270MG
72 175MG
73 280MG
74 185MG
75 18MG
76 1EQ 1.5MG BASE/0.5ML (EQ 1.5MG BASE/0.5ML)
77 1EQ 2.5MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
78 1EQ 2MG BASE
79 1EQ 2MG BASE/2ML (EQ 1MG BASE/ML)
80 1EQ 2MG BASE;EQ 0.5MG BASE
81 1EQ 5MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
82 1EQ 7.5MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
83 1EQ 8MG BASE
84 1EQ 8MG BASE;EQ 2MG BASE
01 35DISCN
02 97RX
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 : AA
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 : 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 : 300MG;7.5MG
Approval Date : 2018-03-30
Application Number : 207808
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 : 300MG;10MG
Approval Date : 2018-03-30
Application Number : 207808
RX/OTC/DISCN : RX
RLD : No
TE Code : AA
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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