01 1AMINOCAPROIC ACID
02 4AMPICILLIN/AMPICILLIN TRIHYDRATE
03 3CEFIXIME
04 2CEPHALEXIN
05 1CHLORZOXAZONE
06 1DESLORATADINE
07 2ESOMEPRAZOLE STRONTIUM
08 1GABAPENTIN
09 1LEVETIRACETAM
10 1MEFENAMIC ACID
11 4PENICILLIN V POTASSIUM
12 3POTASSIUM CHLORIDE
13 1SODIUM POLYSTYRENE SULFONATE
14 3TACROLIMUS
01 2CAPSULE, DELAYED RELEASE;ORAL
02 8CAPSULE;ORAL
03 3FOR SOLUTION;ORAL
04 5FOR SUSPENSION;ORAL
05 1POWDER;ORAL, RECTAL
06 5SOLUTION;ORAL
07 4TABLET;ORAL
01 10.25GM/ML
02 1100MG/5ML
03 1100MG/ML
04 1200MG/5ML
05 120MEQ
06 120MEQ/15ML
07 124.65MG
08 2250MG
09 1250MG/5ML
10 140MEQ/15ML
11 1454GM/BOT
12 149.3MG
13 1500MG/5ML
14 15MG
15 1EQ 0.5MG BASE
16 2EQ 125MG BASE/5ML
17 1EQ 1MG BASE
18 3EQ 250MG BASE
19 2EQ 250MG BASE/5ML
20 3EQ 500MG BASE
21 1EQ 5MG BASE
01 10DISCN
02 18RX
RLD : No
TE Code : AA
Dosage Form : SOLUTION; ORAL
Proprietary Name : AMINOCAPROIC ACID
Dosage Strength : 0.25GM/ML
Approval Date : 2021-04-08
Application Number : 213825
RX/OTC/DISCN : RX
RLD : No
TE Code : AA
RLD : No
TE Code :
AMPICILLIN/AMPICILLIN TRIHYDRATE
Dosage Form : FOR SUSPENSION; ORAL
Proprietary Name : AMPICILLIN TRIHYDRATE
Dosage Strength : EQ 125MG BASE/5ML
Approval Date : 1982-01-01
Application Number : 61601
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
AMPICILLIN/AMPICILLIN TRIHYDRATE
Dosage Form : FOR SUSPENSION; ORAL
Proprietary Name : AMPICILLIN TRIHYDRATE
Dosage Strength : EQ 250MG BASE/5ML
Approval Date : 1982-01-01
Application Number : 61601
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
AMPICILLIN/AMPICILLIN TRIHYDRATE
Dosage Form : CAPSULE; ORAL
Proprietary Name : AMPICILLIN TRIHYDRATE
Dosage Strength : EQ 250MG BASE
Approval Date : 1982-01-01
Application Number : 61602
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
AMPICILLIN/AMPICILLIN TRIHYDRATE
Dosage Form : CAPSULE; ORAL
Proprietary Name : AMPICILLIN TRIHYDRATE
Dosage Strength : EQ 500MG BASE
Approval Date : 1982-01-01
Application Number : 61602
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code : AB
Dosage Form : FOR SUSPENSION; ORAL
Proprietary Name : CEFIXIME
Dosage Strength : 100MG/5ML
Approval Date : 2017-02-06
Application Number : 206938
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : FOR SUSPENSION; ORAL
Proprietary Name : CEFIXIME
Dosage Strength : 200MG/5ML
Approval Date : 2017-02-06
Application Number : 206938
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : FOR SUSPENSION; ORAL
Proprietary Name : CEFIXIME
Dosage Strength : 500MG/5ML
Approval Date : 2017-02-06
Application Number : 206939
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : CAPSULE; ORAL
Proprietary Name : CEPHALEXIN
Dosage Strength : EQ 250MG BASE
Approval Date : 1988-07-15
Application Number : 62713
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : CAPSULE; ORAL
Proprietary Name : CEPHALEXIN
Dosage Strength : EQ 500MG BASE
Approval Date : 1988-07-15
Application Number : 62713
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
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