01 1ADAGRASIB
02 5AMPICILLIN SODIUM
03 7AMPICILLIN/AMPICILLIN TRIHYDRATE
04 1AMPICILLIN/AMPICILLIN TRIHYDRATE; PROBENECID
05 4APIXABAN
06 1ATAZANAVIR SULFATE; COBICISTAT
07 2AZACITIDINE
08 5CEFADROXIL/CEFADROXIL HEMIHYDRATE
09 5CEFORANIDE
10 3CEPHALOTHIN SODIUM
11 1DEUCRAVACITINIB
12 1DIDANOSINE
13 2ERYTHROMYCIN STEARATE
14 1GENTAMICIN SULFATE
15 4HETACILLIN
16 2HETACILLIN POTASSIUM
17 4Levetiracetam
18 4MAVACAMTEN
19 4METHOTREXATE SODIUM
20 2MITOMYCIN
21 3OZANIMOD HYDROCHLORIDE
22 2PENICILLIN V POTASSIUM
23 4POMALIDOMIDE
24 2REPOTRECTINIB
25 6STAVUDINE
26 1Sumatriptan Succinate
27 4TETRACYCLINE HYDROCHLORIDE
28 7TETRACYCLINE PHOSPHATE COMPLEX
29 2Zolpidem Tartrate
01 83BRISTOL
02 7Bristol Lab. Ltd.
01 34CAPSULE;ORAL
02 2FOR SOLUTION;ORAL
03 13FOR SUSPENSION;ORAL
04 7Film Coated Tablet
05 20INJECTABLE;INJECTION
06 1SUSPENSION;ORAL
07 1TABLET, CHEWABLE;ORAL
08 12TABLET;ORAL
01 20.15MG
02 10.5MG
03 11000mg
04 110GM/VIAL
05 110MG
06 110MG/ML
07 110mg
08 115MG
09 115MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
10 1160MG
11 11GM/VIAL
12 11MG
13 11MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
14 12.5MG
15 2200MG
16 120GM/VIAL
17 120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
18 120MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
19 2250MG
20 1250mg
21 12GM/VIAL
22 12MG
23 1300MG
24 130MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
25 13MG
26 140MG
27 140MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
28 14MG
29 2500MG
30 1500MG/VIAL
31 1500mg
32 150mg
33 35MG
34 15MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
35 15mg
36 16MG
37 1750mg
38 1EQ 0.23MG BASE
39 1EQ 0.46MG BASE
40 1EQ 0.92MG BASE
41 1EQ 100MG BASE/ML
42 1EQ 100MG BASE/VIAL
43 1EQ 100MG HYDROCHLORIDE
44 1EQ 112.5MG AMPICIL/5ML
45 2EQ 112.5MG AMPICIL/ML
46 1EQ 125MG BASE
47 2EQ 125MG BASE/5ML
48 1EQ 125MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
49 1EQ 1GM BASE
50 1EQ 1GM BASE/VIAL
51 1EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
52 1EQ 20MG BASE/VIAL
53 1EQ 225MG AMPICIL
54 1EQ 225MG AMPICIL/5ML
55 4EQ 250MG BASE
56 2EQ 250MG BASE/5ML
57 1EQ 250MG BASE/VIAL
58 1EQ 250MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
59 3EQ 250MG HYDROCHLORIDE
60 1EQ 2GM BASE/VIAL
61 1EQ 2GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
62 1EQ 3.5GM BASE/BOT;1GM/BOT
63 1EQ 300MG BASE;150MG
64 1EQ 40MG BASE/ML
65 1EQ 450MG AMPICIL
66 1EQ 4GM BASE/VIAL
67 3EQ 500MG BASE
68 2EQ 500MG BASE/5ML
69 1EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
70 3EQ 500MG HYDROCHLORIDE
71 1EQ 50MG BASE/VIAL
01 7Sweden
02 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).
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