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01 1ACETAMINOPHEN
02 1BUMETANIDE
03 3BUPIVACAINE HYDROCHLORIDE
04 1CHLORPROMAZINE HYDROCHLORIDE
05 2DAPTOMYCIN
06 1DOXYCYCLINE HYCLATE
07 1FOSAPREPITANT DIMEGLUMINE
08 1FUROSEMIDE
09 2KETOROLAC TROMETHAMINE
10 1LACOSAMIDE
11 4LIDOCAINE HYDROCHLORIDE
12 4MAGNESIUM SULFATE
13 2MICAFUNGIN SODIUM
14 1NOREPINEPHRINE BITARTRATE
15 1OLANZAPINE
16 1PANTOPRAZOLE SODIUM
17 3PHENYLEPHRINE HYDROCHLORIDE
18 1POSACONAZOLE
19 1PROPOFOL
20 2ROCURONIUM BROMIDE
21 2SELENIOUS ACID
22 1SUCCINYLCHOLINE CHLORIDE
23 2SUGAMMADEX SODIUM
24 1THIAMINE HYDROCHLORIDE
25 2VANCOMYCIN HYDROCHLORIDE
26 1VERAPAMIL HYDROCHLORIDE
27 1VORICONAZOLE
28 3ZINC SULFATE
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01 47ASPIRO
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01 22INJECTABLE;INJECTION
02 3INJECTABLE;INTRAVENOUS
03 1POWDER;INTRAMUSCULAR
04 4POWDER;INTRAVENOUS
05 4SOLUTION;INTRAMUSCULAR, INTRAVENOUS
06 13SOLUTION;INTRAVENOUS
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01 10.25%
02 10.25MG/ML
03 10.5%
04 10.75%
05 21%
06 2100MG/10ML (10MG/ML)
07 1100MG/ML
08 110GM/20ML (500MG/ML)
09 210MG/ML
10 110MG/ML (10MG/ML)
11 110MG/VIAL
12 115MG/ML
13 11GM/100ML (10MG/ML)
14 11GM/2ML (500MG/ML)
15 22%
16 12.5MG/ML
17 1200MG/20ML (10MG/ML)
18 1200MG/VIAL
19 120MG/ML
20 125GM/50ML (500MG/ML)
21 125MG/ML
22 1300MG/16.7ML (18MG/ML)
23 130MG/ML
24 1350MG/VIAL
25 1500MG/VIAL
26 250MG/5ML (10MG/ML)
27 15GM/10ML (500MG/ML)
28 2EQ 100MG BASE/VIAL
29 1EQ 10MG BASE/10ML (EQ 1MG BASE/ML)
30 1EQ 12MCG SELENIUM/2ML (EQ 6MCG SELENIUM/ML)
31 1EQ 150MG BASE/VIAL
32 1EQ 1GM BASE/VIAL
33 1EQ 1MG BASE/ML
34 1EQ 200MG BASE/2ML (EQ 100MG BASE/ML)
35 1EQ 25MG BASE/5ML (EQ 5MG BASE/ML)
36 1EQ 30MG BASE/10ML (EQ 3MG BASE/ML)
37 1EQ 40MG BASE/VIAL
38 1EQ 500MG BASE/5ML (EQ 100MG BASE/ML)
39 1EQ 500MG BASE/VIAL
40 1EQ 50MG BASE/VIAL
41 1EQ 600MCG SELENIUM/10ML (EQ 60MCG SELENIUM/ML)
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01 47USA
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Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION;INTRAVENOUS
Brand Name : ACETAMINOPHEN
Dosage Strength : 1GM/100ML (10MG/ML)
Packaging :
Approval Date : 2022-07-27
Application Number : 216617
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : BUMETANIDE
Dosage Strength : 0.25MG/ML
Packaging :
Approval Date : 2025-02-27
Application Number : 218746
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : BUPIVACAINE HYDROCHLORIDE
Dosage Strength : 0.25%
Packaging :
Approval Date : 2024-03-27
Application Number : 217821
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : BUPIVACAINE HYDROCHLORIDE
Dosage Strength : 0.5%
Packaging :
Approval Date : 2024-03-27
Application Number : 217821
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : BUPIVACAINE HYDROCHLORIDE
Dosage Strength : 0.75%
Packaging :
Approval Date : 2024-03-27
Application Number : 217821
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : CHLORPROMAZINE HYDROCHLOR...
Dosage Strength : 25MG/ML
Packaging :
Approval Date : 2024-11-18
Application Number : 218272
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : POWDER;INTRAVENOUS
Brand Name : DAPTOMYCIN
Dosage Strength : 500MG/VIAL
Packaging :
Approval Date : 2022-09-23
Application Number : 216413
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : POWDER;INTRAVENOUS
Brand Name : DAPTOMYCIN
Dosage Strength : 350MG/VIAL
Packaging :
Approval Date : 2022-12-23
Application Number : 216445
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : DOXYCYCLINE HYCLATE
Dosage Strength : EQ 100MG BASE/VIAL
Packaging :
Approval Date : 2025-08-05
Application Number : 218888
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : POWDER;INTRAVENOUS
Brand Name : FOSAPREPITANT DIMEGLUMINE
Dosage Strength : EQ 150MG BASE/VIAL
Packaging :
Approval Date : 2021-07-29
Application Number : 214616
Regulatory Info : RX
Registration Country : USA
