01 1ADAGRASIB
02 5AMPICILLIN SODIUM
03 7AMPICILLIN/AMPICILLIN TRIHYDRATE
04 1AMPICILLIN/AMPICILLIN TRIHYDRATE; PROBENECID
05 1ATAZANAVIR SULFATE; COBICISTAT
06 2AZACITIDINE
07 5CEFADROXIL/CEFADROXIL HEMIHYDRATE
08 5CEFORANIDE
09 3CEPHALOTHIN SODIUM
10 1DEUCRAVACITINIB
11 1DIDANOSINE
12 2ERYTHROMYCIN STEARATE
13 1GENTAMICIN SULFATE
14 4HETACILLIN
15 2HETACILLIN POTASSIUM
16 4MAVACAMTEN
17 4METHOTREXATE SODIUM
18 2MITOMYCIN
19 3OZANIMOD HYDROCHLORIDE
20 2PENICILLIN V POTASSIUM
21 4POMALIDOMIDE
22 2REPOTRECTINIB
23 6STAVUDINE
24 4TETRACYCLINE HYDROCHLORIDE
25 7TETRACYCLINE PHOSPHATE COMPLEX
01 34CAPSULE;ORAL
02 2FOR SOLUTION;ORAL
03 12FOR SUSPENSION;ORAL
04 20INJECTABLE;INJECTION
05 1TABLET, CHEWABLE;ORAL
06 10TABLET;ORAL
01 110GM/VIAL
02 110MG
03 110MG/ML
04 115MG
05 115MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
06 1160MG
07 11GM/VIAL
08 11MG
09 11MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
10 12.5MG
11 2200MG
12 120GM/VIAL
13 120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
14 120MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
15 2250MG
16 12GM/VIAL
17 12MG
18 1300MG
19 130MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
20 13MG
21 140MG
22 140MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
23 14MG
24 2500MG
25 1500MG/VIAL
26 25MG
27 15MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
28 16MG
29 1EQ 0.23MG BASE
30 1EQ 0.46MG BASE
31 1EQ 0.92MG BASE
32 1EQ 100MG BASE/ML
33 1EQ 100MG BASE/VIAL
34 1EQ 100MG HYDROCHLORIDE
35 1EQ 112.5MG AMPICIL/5ML
36 2EQ 112.5MG AMPICIL/ML
37 1EQ 125MG BASE
38 2EQ 125MG BASE/5ML
39 1EQ 125MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
40 1EQ 1GM BASE
41 1EQ 1GM BASE/VIAL
42 1EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
43 1EQ 20MG BASE/VIAL
44 1EQ 225MG AMPICIL
45 1EQ 225MG AMPICIL/5ML
46 4EQ 250MG BASE
47 2EQ 250MG BASE/5ML
48 1EQ 250MG BASE/VIAL
49 1EQ 250MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
50 3EQ 250MG HYDROCHLORIDE
51 1EQ 2GM BASE/VIAL
52 1EQ 2GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
53 1EQ 3.5GM BASE/BOT;1GM/BOT
54 1EQ 300MG BASE;150MG
55 1EQ 40MG BASE/ML
56 1EQ 450MG AMPICIL
57 1EQ 4GM BASE/VIAL
58 3EQ 500MG BASE
59 2EQ 500MG BASE/5ML
60 1EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
61 3EQ 500MG HYDROCHLORIDE
62 1EQ 50MG BASE/VIAL
01 61DISCN
02 18RX
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : KRAZATI
Dosage Strength : 200MG
Approval Date : 2022-12-12
Application Number : 216340
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : No
TE Code :
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : POLYCILLIN-N
Dosage Strength : EQ 125MG BASE/VIAL **Fed...
Approval Date : 1982-01-01
Application Number : 50309
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : POLYCILLIN-N
Dosage Strength : EQ 250MG BASE/VIAL **Fed...
Approval Date : 1982-01-01
Application Number : 50309
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : POLYCILLIN-N
Dosage Strength : EQ 500MG BASE/VIAL **Fed...
Approval Date : 1982-01-01
Application Number : 50309
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : POLYCILLIN-N
Dosage Strength : EQ 1GM BASE/VIAL **Feder...
Approval Date : 1982-01-01
Application Number : 50309
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : POLYCILLIN-N
Dosage Strength : EQ 2GM BASE/VIAL **Feder...
Approval Date : 1982-01-01
Application Number : 50309
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
AMPICILLIN/AMPICILLIN TRIHYDRATE
Dosage Form : TABLET, CHEWABLE; ORAL
Proprietary Name : POLYCILLIN
Dosage Strength : EQ 125MG BASE
Approval Date : 1982-01-01
Application Number : 50093
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
AMPICILLIN/AMPICILLIN TRIHYDRATE
Dosage Form : FOR SUSPENSION; ORAL
Proprietary Name : POLYCILLIN
Dosage Strength : EQ 125MG BASE/5ML
Approval Date : 1982-01-01
Application Number : 50308
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
AMPICILLIN/AMPICILLIN TRIHYDRATE
Dosage Form : FOR SUSPENSION; ORAL
Proprietary Name : POLYCILLIN
Dosage Strength : EQ 250MG BASE/5ML
Approval Date : 1982-01-01
Application Number : 50308
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
AMPICILLIN/AMPICILLIN TRIHYDRATE
Dosage Form : FOR SUSPENSION; ORAL
Proprietary Name : POLYCILLIN
Dosage Strength : EQ 500MG BASE/5ML
Approval Date : 1982-01-01
Application Number : 50308
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
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