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 4MAVACAMTEN
18 4METHOTREXATE SODIUM
19 2MITOMYCIN
20 3OZANIMOD HYDROCHLORIDE
21 2PENICILLIN V POTASSIUM
22 4POMALIDOMIDE
23 2REPOTRECTINIB
24 6STAVUDINE
25 4TETRACYCLINE HYDROCHLORIDE
26 7TETRACYCLINE PHOSPHATE COMPLEX
01 83BRISTOL
01 34CAPSULE;ORAL
02 2FOR SOLUTION;ORAL
03 13FOR SUSPENSION;ORAL
04 20INJECTABLE;INJECTION
05 1SUSPENSION;ORAL
06 1TABLET, CHEWABLE;ORAL
07 12TABLET;ORAL
01 20.15MG
02 10.5MG
03 110GM/VIAL
04 110MG
05 110MG/ML
06 115MG
07 115MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
08 1160MG
09 11GM/VIAL
10 11MG
11 11MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
12 12.5MG
13 2200MG
14 120GM/VIAL
15 120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
16 120MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
17 2250MG
18 12GM/VIAL
19 12MG
20 1300MG
21 130MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
22 13MG
23 140MG
24 140MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
25 14MG
26 2500MG
27 1500MG/VIAL
28 35MG
29 15MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
30 16MG
31 1EQ 0.23MG BASE
32 1EQ 0.46MG BASE
33 1EQ 0.92MG BASE
34 1EQ 100MG BASE/ML
35 1EQ 100MG BASE/VIAL
36 1EQ 100MG HYDROCHLORIDE
37 1EQ 112.5MG AMPICIL/5ML
38 2EQ 112.5MG AMPICIL/ML
39 1EQ 125MG BASE
40 2EQ 125MG BASE/5ML
41 1EQ 125MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
42 1EQ 1GM BASE
43 1EQ 1GM BASE/VIAL
44 1EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
45 1EQ 20MG BASE/VIAL
46 1EQ 225MG AMPICIL
47 1EQ 225MG AMPICIL/5ML
48 4EQ 250MG BASE
49 2EQ 250MG BASE/5ML
50 1EQ 250MG BASE/VIAL
51 1EQ 250MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
52 3EQ 250MG HYDROCHLORIDE
53 1EQ 2GM BASE/VIAL
54 1EQ 2GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
55 1EQ 3.5GM BASE/BOT;1GM/BOT
56 1EQ 300MG BASE;150MG
57 1EQ 40MG BASE/ML
58 1EQ 450MG AMPICIL
59 1EQ 4GM BASE/VIAL
60 3EQ 500MG BASE
61 2EQ 500MG BASE/5ML
62 1EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
63 3EQ 500MG HYDROCHLORIDE
64 1EQ 50MG BASE/VIAL
01 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 : 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 100MG BASE/ML
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 : CAPSULE;ORAL
Brand Name : POLYCILLIN
Dosage Strength : EQ 500MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 50310
Regulatory Info : DISCN
Registration Country : USA
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