01 2ACETYLCYSTEINE
02 2CAFFEINE CITRATE
03 1CUPRIC CHLORIDE
04 2CYSTEINE HYDROCHLORIDE
05 2DICLOFENAC SODIUM; MISOPROSTOL
06 2DILTIAZEM HYDROCHLORIDE
07 2EPHEDRINE SULFATE
08 1ERYTHROMYCIN LACTOBIONATE
09 2FENTANYL CITRATE
10 1GANCICLOVIR
11 4GLYCOPYRROLATE
12 1MAGNESIUM SULFATE
13 2MIDAZOLAM
14 3NEOSTIGMINE METHYLSULFATE
15 3PHENYLEPHRINE HYDROCHLORIDE
16 2POTASSIUM ACETATE
17 3SODIUM BICARBONATE
18 3SODIUM NITROPRUSSIDE
19 1TRANEXAMIC ACID
20 2VERAPAMIL HYDROCHLORIDE
21 1ZINC CHLORIDE
01 2EXELA HOLDINGS
02 39EXELA PHARMA
03 1EXELA PHARMA SCIENCE
01 8INJECTABLE;INJECTION
02 1INJECTABLE;INTRAVENOUS
03 1SOLUTION;INHALATION, ORAL
04 5SOLUTION;INTRAMUSCULAR, INTRAVENOUS
05 24SOLUTION;INTRAVENOUS
06 1SOLUTION;ORAL
07 2TABLET, DELAYED RELEASE;ORAL
01 10.2MG/ML (0.2MG/ML)
02 10.4MG/2ML (0.2MG/ML)
03 10.5MEQ/ML
04 10.6MG/3ML (0.2MG/ML)
05 10.9MEQ/ML
06 1100MG/100ML (1MG/ML)
07 1100MG/10ML (10MG/ML)
08 110MG/10ML (1MG/ML)
09 110MG/4ML (2.5MG/ML)
10 110MG/50ML (0.2MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
11 110MG/ML (10MG/ML)
12 1125MG/125ML (1MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
13 11GM/100ML (10MG/ML)
14 11MEQ/ML
15 11MG/5ML (0.2MG/ML)
16 120%
17 120MG/100ML (0.2MG/ML)
18 12500MG/50ML (50MG/ML)
19 1250MG/250ML (1MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
20 125MG/5ML (5MG/ML)
21 22MEQ/ML
22 1500MG/10ML (50MG/ML)
23 1500MG/250ML (2MG/ML)
24 150MG/100ML (0.5MG/ML)
25 150MG/50ML (1MG/ML)
26 150MG/5ML (10MG/ML)
27 150MG/ML (50MG/ML)
28 150MG;0.2MG
29 15GM/10ML (500MG/ML)
30 15MG/10ML (0.5MG/ML)
31 15MG/2ML (2.5MG/ML)
32 15MG/5ML (1MG/ML)
33 16GM/30ML (200MG/ML)
34 175MG;0.2MG
35 1EQ 0.4MG COPPER/ML
36 1EQ 1MG ZINC/ML
37 1EQ 2.5MG BASE/50ML (EQ 0.05MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
38 2EQ 30MG BASE/3ML (EQ 10MG BASE/ML)
39 1EQ 500MG BASE/VIAL
40 1EQ 5MG BASE/100ML (EQ 0.05MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
01 42USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INTRAVENOUS
Brand Name : ACETYLCYSTEINE
Dosage Strength : 6GM/30ML (200MG/ML)
Packaging :
Approval Date : 2021-04-15
Application Number : 204797
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : SOLUTION;INHALATION, ORA...
Brand Name : ACETYLCYSTEINE
Dosage Strength : 20%
Packaging :
Approval Date : 2023-11-01
Application Number : 205643
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION;INTRAVENOUS
Brand Name : CAFFEINE CITRATE
Dosage Strength : EQ 30MG BASE/3ML (EQ 1...
Packaging :
Approval Date : 2006-09-21
Application Number : 77233
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION;ORAL
Brand Name : CAFFEINE CITRATE
Dosage Strength : EQ 30MG BASE/3ML (EQ 1...
Packaging :
Approval Date : 2006-09-21
Application Number : 77304
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : CUPRIC CHLORIDE
Dosage Strength : EQ 0.4MG COPPER/ML
Packaging :
Approval Date : 2022-10-31
Application Number : 212071
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION;INTRAVENOUS
Brand Name : ELCYS
Dosage Strength : 500MG/10ML (50MG/ML)
Packaging :
Approval Date : 2019-04-16
Application Number : 210660
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : SOLUTION;INTRAVENOUS
Brand Name : ELCYS
Dosage Strength : 2500MG/50ML (50MG/ML)
Packaging :
Approval Date : 2023-12-04
Application Number : 210660
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
DICLOFENAC SODIUM; MISOPROSTOL
Dosage Form : TABLET, DELAYED RELEASE;...
Brand Name : DICLOFENAC SODIUM AND MIS...
Dosage Strength : 50MG;0.2MG
Packaging :
Approval Date : 2014-03-14
Application Number : 200540
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
DICLOFENAC SODIUM; MISOPROSTOL
Dosage Form : TABLET, DELAYED RELEASE;...
Brand Name : DICLOFENAC SODIUM AND MIS...
Dosage Strength : 75MG;0.2MG
Packaging :
Approval Date : 2014-03-14
Application Number : 200540
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : SOLUTION;INTRAVENOUS
Brand Name : DILTIAZEM HYDROCHLORIDE I...
Dosage Strength : 250MG/250ML (1MG/ML) *...
Packaging :
Approval Date : 2021-10-28
Application Number : 215252
Regulatory Info : DISCN
Registration Country : USA
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