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01 2ACETAMINOPHEN; BUTALBITAL
02 1CAFFEINE; ERGOTAMINE TARTRATE
03 1CALCITRIOL
04 3CEFDINIR
05 2CEFPODOXIME PROXETIL
06 1CEFTRIAXONE SODIUM
07 3CEFUROXIME AXETIL
08 2CEPHALEXIN
09 3CHLORZOXAZONE
10 1DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM
11 1FLUOCINOLONE ACETONIDE
12 2LEVETIRACETAM
13 1LORATADINE
14 2METHAZOLAMIDE
15 2METHYLPHENIDATE HYDROCHLORIDE
16 6MORPHINE SULFATE
17 2OMEPRAZOLE; SODIUM BICARBONATE
18 3POTASSIUM CHLORIDE
19 1PREGABALIN
20 4PROPRANOLOL HYDROCHLORIDE
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01 10CAPSULE, EXTENDED RELEASE;ORAL
02 5CAPSULE;ORAL
03 1FOR SOLUTION;ORAL
04 2FOR SUSPENSION;ORAL
05 1INJECTABLE;INJECTION
06 1OIL/DROPS;OTIC
07 6SOLUTION;ORAL
08 1SOLUTION;ORAL, RECTAL
09 2TABLET, EXTENDED RELEASE;ORAL
10 14TABLET;ORAL
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01 10.01%
02 1100MG
03 1100MG;1MG
04 110MG
05 110MG/5ML
06 1120MG
07 1125MG/5ML
08 1160MG
09 11MCG/ML
10 120MEQ
11 120MEQ/15ML
12 120MG
13 120MG/ML
14 120MG;1.1GM
15 1250MG
16 1250MG/5ML
17 125MG
18 1300MG
19 1300MG;50MG
20 130MG
21 1325MG;50MG
22 1375MG
23 140MEQ/15ML
24 140MG;1.1GM
25 1500MG
26 250MG
27 15MG/5ML
28 260MG
29 166%;10%
30 2750MG
31 280MG
32 1EQ 100MG BASE
33 1EQ 10GM BASE/VIAL
34 1EQ 125MG BASE
35 1EQ 200MG BASE
36 2EQ 250MG BASE
37 2EQ 500MG BASE
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01 6DISCN
02 1OTC
03 36RX
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RLD : No
TE Code : AA
Dosage Form : TABLET; ORAL
Proprietary Name : BUTAPAP
Dosage Strength : 325MG;50MG
Approval Date : 1992-10-26
Application Number : 89987
RX/OTC/DISCN : RX
RLD : No
TE Code : AA

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RLD : No
TE Code : AA
Dosage Form : TABLET; ORAL
Proprietary Name : BUTALBITAL AND ACETAMINO...
Dosage Strength : 300MG;50MG
Approval Date : 2016-11-15
Application Number : 207386
RX/OTC/DISCN : RX
RLD : No
TE Code : AA

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RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : ERGOTAMINE TARTRATE AND ...
Dosage Strength : 100MG;1MG
Approval Date : 2005-09-16
Application Number : 40590
RX/OTC/DISCN : RX
RLD : No
TE Code :

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RLD : No
TE Code : AA
Dosage Form : SOLUTION; ORAL
Proprietary Name : CALCITRIOL
Dosage Strength : 1MCG/ML
Approval Date : 2023-07-28
Application Number : 203973
RX/OTC/DISCN : RX
RLD : No
TE Code : AA

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RLD : No
TE Code : AB
Dosage Form : CAPSULE; ORAL
Proprietary Name : CEFDINIR
Dosage Strength : 300MG
Approval Date : 2007-07-18
Application Number : 65418
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : FOR SUSPENSION; ORAL
Proprietary Name : CEFDINIR
Dosage Strength : 125MG/5ML
Approval Date : 2007-07-18
Application Number : 65429
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : FOR SUSPENSION; ORAL
Proprietary Name : CEFDINIR
Dosage Strength : 250MG/5ML
Approval Date : 2007-07-18
Application Number : 65429
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : CEFPODOXIME PROXETIL
Dosage Strength : EQ 100MG BASE
Approval Date : 2007-11-14
Application Number : 65388
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : CEFPODOXIME PROXETIL
Dosage Strength : EQ 200MG BASE
Approval Date : 2007-11-14
Application Number : 65388
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AP
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : CEFTRIAXONE SODIUM
Dosage Strength : EQ 10GM BASE/VIAL
Approval Date : 2017-01-20
Application Number : 91117
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
