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01 1STRIDES PHARMA INTL
02 1ACTAVIS MID ATLANTIC
03 1AM THERAP
04 1ANVI
05 1APPCO
06 1ASCOT
07 1CHARTWELL MOLECULAR
08 2CHARTWELL RX
09 1DURAMED PHARMS BARR
10 2HALSEY
11 1HERITAGE PHARMA
12 1INGENUS PHARMS LLC
13 1KENTON
14 1KV PHARM
15 1MD PHARM
16 2MERCK
17 1MORTON GROVE
18 1MOUNTAIN
19 1MYLAN
20 1NASKA
21 1PATRIN
22 1PHARM ASSOC
23 1PIONEER PHARMS
24 1PLIVA
25 2QUAGEN
26 1REGCON HOLDINGS
27 3RISING
28 1ST JOHN PHARM
29 1SUPERPHARM
30 1TRIS PHARMA INC
31 1VITARINE
32 3WATSON LABS
33 1ZYDUS PHARMS
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01 12SYRUP;ORAL
02 29TABLET;ORAL
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01 27DISCN
02 14RX
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01 39CYPROHEPTADINE HYDROCHLORIDE
02 2PERIACTIN
01 37No
02 4Yes
RLD : No
TE Code : AA
Brand Name : CYPROHEPTADINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 4MG
Approval Date : 2018-04-11
Application Number : 209172
RX/OTC/DISCN : RX
RLD : No
TE Code : AA
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RLD : No
TE Code :
Brand Name : CYPROHEPTADINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 4MG
Approval Date : 1982-01-01
Application Number : 85245
RX/OTC/DISCN : DISCN
RLD : No
TE Code :

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RLD : No
TE Code :
Brand Name : CYPROHEPTADINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 4MG
Approval Date : 1982-01-01
Application Number : 86165
RX/OTC/DISCN : DISCN
RLD : No
TE Code :

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RLD : No
TE Code :
Brand Name : CYPROHEPTADINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 4MG
Approval Date : 1982-01-01
Application Number : 86580
RX/OTC/DISCN : DISCN
RLD : No
TE Code :

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RLD : No
TE Code : AA
Brand Name : CYPROHEPTADINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 4MG
Approval Date : 2006-05-30
Application Number : 40644
RX/OTC/DISCN : RX
RLD : No
TE Code : AA

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RLD : Yes
TE Code :
Brand Name : PERIACTIN
Dosage Form : TABLET;ORAL
Dosage Strength : 4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 12649
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :

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RLD : Yes
TE Code :
Brand Name : PERIACTIN
Dosage Form : SYRUP;ORAL
Dosage Strength : 2MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 13220
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :

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RLD : No
TE Code : AA
Brand Name : CYPROHEPTADINE HYDROCHLORIDE
Dosage Form : SYRUP;ORAL
Dosage Strength : 2MG/5ML
Approval Date : 2006-06-28
Application Number : 40668
RX/OTC/DISCN : RX
RLD : No
TE Code : AA

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RLD : No
TE Code :
Brand Name : CYPROHEPTADINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 4MG
Approval Date : 1982-01-01
Application Number : 86678
RX/OTC/DISCN : DISCN
RLD : No
TE Code :

Brand Name : CYPROHEPTADINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 4MG
Approval Date : 2003-09-30
Application Number : 40537
RX/OTC/DISCN : RX
RLD : No
TE Code : AA

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