01 1ACETYLCYSTEINE
02 5AMPICILLIN SODIUM
03 3AMPICILLIN SODIUM; SULBACTAM SODIUM
04 5BUPIVACAINE HYDROCHLORIDE
05 1CARBOPROST TROMETHAMINE
06 1FOSAPREPITANT DIMEGLUMINE
07 1GANCICLOVIR SODIUM
08 4KETOROLAC TROMETHAMINE
09 1LABETALOL HYDROCHLORIDE
10 3LEVOTHYROXINE SODIUM
11 1METHOHEXITAL SODIUM
12 1METHYLENE BLUE
13 1METOPROLOL TARTRATE
14 4MIDAZOLAM HYDROCHLORIDE
15 1MYCOPHENOLATE MOFETIL HYDROCHLORIDE
16 2NAFCILLIN SODIUM
17 2ONDANSETRON HYDROCHLORIDE
18 2OXACILLIN SODIUM
19 3PIPERACILLIN SODIUM; TAZOBACTAM SODIUM
20 1ROCURONIUM BROMIDE
21 1SODIUM BICARBONATE
22 1SUCCINYLCHOLINE CHLORIDE
23 3SUMATRIPTAN SUCCINATE
24 1THIAMINE HYDROCHLORIDE
25 9VANCOMYCIN HYDROCHLORIDE
01 8STERISCIENCE
02 50STERISCIENCE SPECLTS
01 48INJECTABLE;INJECTION
02 1INJECTABLE;INTRAVENOUS
03 3INJECTABLE;SUBCUTANEOUS
04 3POWDER;INTRAVENOUS
05 1SOLUTION;INTRAMUSCULAR, INTRAVENOUS
06 2SOLUTION;INTRAVENOUS
01 20.25%
02 20.5%
03 10.75%
04 1100MCG/VIAL
05 1100MG/5ML (20MG/ML)
06 1100MG/ML
07 215MG/ML
08 11MEQ/ML
09 11MG/ML
10 1200MCG/VIAL
11 230MG/ML
12 1500MCG/VIAL
13 2500MG/VIAL
14 150MG/10ML (5MG/ML)
15 150MG/5ML (10MG/ML)
16 15MG/ML
17 16GM/30ML (200MG/ML)
18 1EQ 0.25MG BASE/ML
19 1EQ 10GM BASE/VIAL
20 1EQ 10GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
21 1EQ 10GM BASE/VIAL;EQ 5GM BASE/VIAL
22 1EQ 150MG BASE/50ML (EQ 3MG BASE/ML)
23 5EQ 1GM BASE/VIAL
24 2EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
25 1EQ 1GM BASE/VIAL;EQ 500MG BASE/VIAL
26 2EQ 1MG BASE/ML
27 1EQ 250MG BASE/VIAL
28 3EQ 2GM BASE/VIAL
29 1EQ 2GM BASE/VIAL;EQ 1GM BASE/VIAL
30 1EQ 2GM BASE/VIAL;EQ 250MG BASE/VIAL
31 2EQ 2MG BASE/ML
32 1EQ 3GM BASE/VIAL;EQ 375MG BASE/VIAL
33 1EQ 4GM BASE/VIAL;EQ 500MG BASE/VIAL
34 4EQ 500MG BASE/VIAL
35 2EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
36 2EQ 5MG BASE/ML
37 3EQ 6MG BASE/0.5ML (EQ 12MG BASE/ML)
01 58USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : INJECTABLE;INTRAVENOUS
Brand Name : ACETYLCYSTEINE
Dosage Strength : 6GM/30ML (200MG/ML)
Packaging :
Approval Date : 2023-04-19
Application Number : 217182
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : AMPICILLIN SODIUM
Dosage Strength : EQ 250MG BASE/VIAL
Packaging :
Approval Date : 2014-04-09
Application Number : 201025
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : AMPICILLIN SODIUM
Dosage Strength : EQ 500MG BASE/VIAL
Packaging :
Approval Date : 2014-04-09
Application Number : 201025
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : AMPICILLIN SODIUM
Dosage Strength : EQ 1GM BASE/VIAL
Packaging :
Approval Date : 2014-04-09
Application Number : 201025
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : AMPICILLIN SODIUM
Dosage Strength : EQ 2GM BASE/VIAL
Packaging :
Approval Date : 2014-04-09
Application Number : 201025
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : AMPICILLIN SODIUM
Dosage Strength : EQ 10GM BASE/VIAL
Packaging :
Approval Date : 2014-04-07
Application Number : 202198
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Dosage Form : INJECTABLE;INJECTION
Brand Name : AMPICILLIN AND SULBACTAM
Dosage Strength : EQ 1GM BASE/VIAL;EQ 50...
Packaging :
Approval Date : 2014-04-07
Application Number : 201024
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Dosage Form : INJECTABLE;INJECTION
Brand Name : AMPICILLIN AND SULBACTAM
Dosage Strength : EQ 2GM BASE/VIAL;EQ 1G...
Packaging :
Approval Date : 2014-04-07
Application Number : 201024
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Dosage Form : INJECTABLE;INJECTION
Brand Name : AMPICILLIN AND SULBACTAM
Dosage Strength : EQ 10GM BASE/VIAL;EQ 5...
Packaging :
Approval Date : 2014-04-07
Application Number : 202197
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : BUPIVACAINE HYDROCHLORIDE
Dosage Strength : 0.25%
Packaging :
Approval Date : 2011-10-18
Application Number : 91503
Regulatory Info : RX
Registration Country : USA
