01 1ADAGRASIB
02 5AMPICILLIN SODIUM
03 7AMPICILLIN/AMPICILLIN TRIHYDRATE
04 1AMPICILLIN/AMPICILLIN TRIHYDRATE; PROBENECID
05 4APIXABAN
06 1ATAZANAVIR SULFATE; COBICISTAT
07 2AZACITIDINE
08 1Aspirin Bp
09 1Bendroflumethiazide
10 5CEFADROXIL/CEFADROXIL HEMIHYDRATE
11 5CEFORANIDE
12 3CEPHALOTHIN SODIUM
13 1DEUCRAVACITINIB
14 1DIDANOSINE
15 1Digoxin
16 2ERYTHROMYCIN STEARATE
17 1GENTAMICIN SULFATE
18 4HETACILLIN
19 2HETACILLIN POTASSIUM
20 4Levetiracetam
21 4MAVACAMTEN
22 4METHOTREXATE SODIUM
23 2MITOMYCIN
24 3OZANIMOD HYDROCHLORIDE
25 2PENICILLIN V POTASSIUM
26 4POMALIDOMIDE
27 2REPOTRECTINIB
28 1Ranitidine Hydrochloride
29 6STAVUDINE
30 1Sumatriptan Succinate
31 4TETRACYCLINE HYDROCHLORIDE
32 7TETRACYCLINE PHOSPHATE COMPLEX
33 1Tramadol Hydrochloride
34 2Zolpidem Tartrate
01 83BRISTOL
02 7Bristol Lab. Ltd.
03 5Bristol Laboratories Limited
01 34CAPSULE;ORAL
02 1Capsule
03 2FOR SOLUTION;ORAL
04 13FOR SUSPENSION;ORAL
05 8Film Coated Tablet
06 1Gastro-Resistant Tablet
07 20INJECTABLE;INJECTION
08 1SUSPENSION;ORAL
09 1TABLET, CHEWABLE;ORAL
10 12TABLET;ORAL
11 2Tablet
01 10.0625MG
02 20.15MG
03 10.5MG
04 11000mg
05 110GM/VIAL
06 110MG
07 110MG/ML
08 110mg
09 115MG
10 115MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
11 1160MG
12 11GM/VIAL
13 11MG
14 11MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
15 22.5MG
16 2200MG
17 120GM/VIAL
18 120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
19 120MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
20 2250MG
21 1250mg
22 12GM/VIAL
23 12MG
24 1300MG
25 130MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
26 13MG
27 140MG
28 140MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
29 14MG
30 2500MG
31 1500MG/VIAL
32 1500mg
33 150MG
34 150mg
35 35MG
36 15MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
37 15mg
38 16MG
39 1750mg
40 275MG
41 1EQ 0.23MG BASE
42 1EQ 0.46MG BASE
43 1EQ 0.92MG BASE
44 1EQ 100MG BASE/ML
45 1EQ 100MG BASE/VIAL
46 1EQ 100MG HYDROCHLORIDE
47 1EQ 112.5MG AMPICIL/5ML
48 2EQ 112.5MG AMPICIL/ML
49 1EQ 125MG BASE
50 2EQ 125MG BASE/5ML
51 1EQ 125MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
52 1EQ 1GM BASE
53 1EQ 1GM BASE/VIAL
54 1EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
55 1EQ 20MG BASE/VIAL
56 1EQ 225MG AMPICIL
57 1EQ 225MG AMPICIL/5ML
58 4EQ 250MG BASE
59 2EQ 250MG BASE/5ML
60 1EQ 250MG BASE/VIAL
61 1EQ 250MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
62 3EQ 250MG HYDROCHLORIDE
63 1EQ 2GM BASE/VIAL
64 1EQ 2GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
65 1EQ 3.5GM BASE/BOT;1GM/BOT
66 1EQ 300MG BASE;150MG
67 1EQ 40MG BASE/ML
68 1EQ 450MG AMPICIL
69 1EQ 4GM BASE/VIAL
70 3EQ 500MG BASE
71 2EQ 500MG BASE/5ML
72 1EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
73 3EQ 500MG HYDROCHLORIDE
74 1EQ 50MG BASE/VIAL
01 5Malta
02 7Sweden
03 83USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : KRAZATI
Dosage Strength : 200MG
Packaging :
Approval Date : 2022-12-12
Application Number : 216340
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : POLYCILLIN-N
Dosage Strength : EQ 125MG BASE/VIAL **F...
Packaging :
Approval Date : 1982-01-01
Application Number : 50309
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : POLYCILLIN-N
Dosage Strength : EQ 250MG BASE/VIAL **F...
Packaging :
Approval Date : 1982-01-01
Application Number : 50309
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : POLYCILLIN-N
Dosage Strength : EQ 500MG BASE/VIAL **F...
Packaging :
Approval Date : 1982-01-01
Application Number : 50309
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : POLYCILLIN-N
Dosage Strength : EQ 1GM BASE/VIAL **Fed...
Packaging :
Approval Date : 1982-01-01
Application Number : 50309
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : POLYCILLIN-N
Dosage Strength : EQ 2GM BASE/VIAL **Fed...
Packaging :
Approval Date : 1982-01-01
Application Number : 50309
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMPICILLIN/AMPICILLIN TRIHYDRATE
Dosage Form : TABLET, CHEWABLE;ORAL
Brand Name : POLYCILLIN
Dosage Strength : EQ 125MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 50093
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMPICILLIN/AMPICILLIN TRIHYDRATE
Dosage Form : FOR SUSPENSION;ORAL
Brand Name : POLYCILLIN
Dosage Strength : EQ 125MG BASE/5ML
Packaging :
Approval Date : 1982-01-01
Application Number : 50308
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMPICILLIN/AMPICILLIN TRIHYDRATE
Dosage Form : FOR SUSPENSION;ORAL
Brand Name : POLYCILLIN
Dosage Strength : EQ 250MG BASE/5ML
Packaging :
Approval Date : 1982-01-01
Application Number : 50308
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMPICILLIN/AMPICILLIN TRIHYDRATE
Dosage Form : FOR SUSPENSION;ORAL
Brand Name : POLYCILLIN
Dosage Strength : EQ 500MG BASE/5ML
Packaging :
Approval Date : 1982-01-01
Application Number : 50308
Regulatory Info : DISCN
Registration Country : USA
Bristol Laboratories Ltd is a supplier offers 4 products (APIs, Excipients or Intermediates).
Find a price of Ceforanide bulk offered by Bristol Laboratories Ltd
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