01 6BUPROPION HYDROCHLORIDE
02 2CHOLINE FENOFIBRATE
03 3DESVENLAFAXINE SUCCINATE
04 2FENOFIBRATE
05 3FLECAINIDE ACETATE
06 4GUANFACINE HYDROCHLORIDE
07 4IBUPROFEN
08 4MEMANTINE HYDROCHLORIDE
09 2METFORMIN HYDROCHLORIDE
10 4METOPROLOL SUCCINATE
11 1NAPROXEN SODIUM
12 3NIACIN
13 4POTASSIUM CHLORIDE
14 3VENLAFAXINE HYDROCHLORIDE
01 2CAPSULE, DELAYED RELEASE;ORAL
02 7CAPSULE, EXTENDED RELEASE;ORAL
03 26TABLET, EXTENDED RELEASE;ORAL
04 10TABLET;ORAL
01 2100MG
02 210MEQ
03 114MG
04 4150MG
05 1160MG
06 11GM
07 2200MG
08 120MEQ
09 121MG
10 1220MG
11 128MG
12 1300MG
13 1400MG
14 2500MG
15 150MG
16 154MG
17 1600MG
18 2750MG
19 17MG
20 1800MG
21 18MEQ
22 1EQ 100MG BASE
23 1EQ 100MG TARTRATE
24 1EQ 135MG FENOFIBRIC ACID
25 1EQ 150MG BASE
26 1EQ 1MG BASE
27 1EQ 200MG TARTRATE
28 1EQ 25MG BASE
29 1EQ 25MG TARTRATE
30 1EQ 2MG BASE
31 1EQ 37.5MG BASE
32 1EQ 3MG BASE
33 1EQ 45MG FENOFIBRIC ACID
34 1EQ 4MG BASE
35 1EQ 50MG BASE
36 1EQ 50MG TARTRATE
37 1EQ 75MG BASE
01 4DISCN
02 1OTC
03 40RX
RLD : No
TE Code : AB3
Yichang Humanwell Pharmaceutical
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : BUPROPION HYDROCHLORIDE
Dosage Strength : 150MG
Approval Date : 2018-06-14
Application Number : 210015
RX/OTC/DISCN : RX
RLD : No
TE Code : AB3
RLD : No
TE Code : AB3
Yichang Humanwell Pharmaceutical
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : BUPROPION HYDROCHLORIDE
Dosage Strength : 300MG
Approval Date : 2018-06-14
Application Number : 210015
RX/OTC/DISCN : RX
RLD : No
TE Code : AB3
RLD : No
TE Code : AB1
Yichang Humanwell Pharmaceutical
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : BUPROPION HYDROCHLORIDE
Dosage Strength : 100MG
Approval Date : 2018-10-16
Application Number : 211347
RX/OTC/DISCN : RX
RLD : No
TE Code : AB1
RLD : No
TE Code : AB1
Yichang Humanwell Pharmaceutical
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : BUPROPION HYDROCHLORIDE
Dosage Strength : 150MG
Approval Date : 2018-10-16
Application Number : 211347
RX/OTC/DISCN : RX
RLD : No
TE Code : AB1
RLD : No
TE Code : AB1
Yichang Humanwell Pharmaceutical
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : BUPROPION HYDROCHLORIDE
Dosage Strength : 200MG
Approval Date : 2018-10-16
Application Number : 211347
RX/OTC/DISCN : RX
RLD : No
TE Code : AB1
RLD : No
TE Code : AB2
Yichang Humanwell Pharmaceutical
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : BUPROPION HYDROCHLORIDE
Dosage Strength : 150MG
Approval Date : 2023-01-09
Application Number : 216766
RX/OTC/DISCN : RX
RLD : No
TE Code : AB2
RLD : No
TE Code : AB
Yichang Humanwell Pharmaceutical
Dosage Form : CAPSULE, DELAYED RELEASE; ORAL
Proprietary Name : FENOFIBRIC ACID
Dosage Strength : EQ 45MG FENOFIBRIC ACID
Approval Date : 2020-12-23
Application Number : 212562
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Yichang Humanwell Pharmaceutical
Dosage Form : CAPSULE, DELAYED RELEASE; ORAL
Proprietary Name : FENOFIBRIC ACID
Dosage Strength : EQ 135MG FENOFIBRIC ACID
Approval Date : 2020-12-23
Application Number : 212562
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Yichang Humanwell Pharmaceutical
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : DESVENLAFAXINE SUCCINATE
Dosage Strength : EQ 50MG BASE
Approval Date : 2018-10-01
Application Number : 210014
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Yichang Humanwell Pharmaceutical
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : DESVENLAFAXINE SUCCINATE
Dosage Strength : EQ 100MG BASE
Approval Date : 2018-10-01
Application Number : 210014
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
Yichang Humanwell Pharmaceutical is a supplier offers 7 products (APIs, Excipients or Intermediates).
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