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ABRAXIS PHARM
FDA Orange Book

DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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Valsynthese, part of the SSE Group, is a CDMO focused on highly energetic and highly hazardous chemistry.

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xyz-pharma-m-2024-10-07

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With Fermion, start the journey of your innovative API.

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Bloomage is a one-stop source for CEP Sodium Hyaluronate and Hyaluronic Acid// FDA-inspected & GMP-certified.

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xyz-pharma-m-2024-10-07

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ABRAXIS PHARM

Contact Details

CONTACT DETAILS
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EVENTS

Webinars & Exhibitions

Webinars & Exhibitions

DIGITAL CONTENT

INTERVIEW #SpeakPharma, VLOG #PharmaReel, DATA COMPILATION #PharmaFlow, 3 NEWS #PharmaBuzz

INTERVIEW #SpeakPharma
VLOG #PharmaReel
DATA COMPILATION #PharmaFlow
3 NEWS #PharmaBuzz

FINISHED DOSAGE FORMULATIONS

140 FDF Dossiers, 140 FDA Orange Book

140 FDF Dossiers
140 FDA Orange Book

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filter Active Ingredients Reset all filters

140 All

01 1AMINOCAPROIC ACID

02 5AMINOPHYLLINE

03 1AMPHOTERICIN B

04 1ASCORBIC ACID; BIOTIN; CYANOCOBALAMIN; DEXPANTHENOL; ERGOCALCIFEROL; FOLIC ACID; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN 5-PHOSPHATE SODIUM; THIAMINE HYDROCHLORIDE; VITAMIN A; VITAMIN E

05 2BRETYLIUM TOSYLATE

06 1CALCIUM GLUCEPTATE

07 4CEFAZOLIN SODIUM

08 2CEPHALOTHIN SODIUM

09 5CEPHAPIRIN SODIUM

10 1CHLORPROMAZINE HYDROCHLORIDE

11 1CHROMIC CHLORIDE

12 3CLINDAMYCIN PHOSPHATE

13 1CUPRIC SULFATE

14 3CYANOCOBALAMIN

15 2DACARBAZINE

16 1DEXAMETHASONE SODIUM PHOSPHATE

17 1DIAZEPAM

18 1DIAZOXIDE

19 1DIGOXIN

20 1DIPHENHYDRAMINE HYDROCHLORIDE

21 5DOPAMINE HYDROCHLORIDE

22 2DROPERIDOL

23 2ERYTHROMYCIN LACTOBIONATE

24 3FLUOROURACIL

25 2FUROSEMIDE

26 1GLYCOPYRROLATE

27 1HALOPERIDOL LACTATE

28 7HEPARIN SODIUM

29 1HYDRALAZINE HYDROCHLORIDE

30 5HYDROCORTISONE SODIUM SUCCINATE

31 1HYDROXOCOBALAMIN

32 1ISOPROTERENOL HYDROCHLORIDE

33 3KANAMYCIN SULFATE

34 1LEUCOVORIN CALCIUM

35 9LIDOCAINE HYDROCHLORIDE

36 1MANGANESE SULFATE

37 1MANNITOL

38 1METARAMINOL BITARTRATE

39 6METHOTREXATE SODIUM

40 1METHYLDOPATE HYDROCHLORIDE

41 10METHYLPREDNISOLONE SODIUM SUCCINATE

42 1METRONIDAZOLE

43 1METRONIDAZOLE HYDROCHLORIDE

44 2NALBUPHINE HYDROCHLORIDE

45 4NALOXONE HYDROCHLORIDE

46 2NANDROLONE DECANOATE

47 2NITROGLYCERIN

48 6POTASSIUM CHLORIDE

49 2PROCAINAMIDE HYDROCHLORIDE

50 4PROCAINE HYDROCHLORIDE

51 2RITODRINE HYDROCHLORIDE

52 3SODIUM CHLORIDE

53 1SODIUM NITROPRUSSIDE

54 2STERILE WATER FOR INJECTION

55 1SULFAMETHOXAZOLE; TRIMETHOPRIM

56 1THIAMINE HYDROCHLORIDE

57 1VERAPAMIL HYDROCHLORIDE

58 1VINBLASTINE SULFATE

59 1VINCRISTINE SULFATE

60 1ZINC SULFATE

filter Dosage Reset all filters

140 All

01 136INJECTABLE;INJECTION

02 2LIQUID;N/A

03 2SOLUTION;INJECTION

filter Dosage Strength Reset all filters

140 All

01 20.02MG/ML

02 10.03MG/ML

03 10.1MG/ML

04 10.25MG/ML

05 20.2MG/ML

06 10.4MG/ML

07 41%

08 21,000 UNITS/ML

09 11.5%

10 210,000 UNITS/ML

11 2100%

12 4100MG/ML

13 1100MG/VIAL

14 410MG/ML

15 110MG/ML;0.006MG/ML;0.5MCG/ML;1.5MG/ML;20 IU/ML;0.04MG/ML;4MG/ML;0.4MG/ML;0.36MG/ML;0.3MG/ML;330 UNITS/ML;1 IU/ML

16 110MG/VIAL

17 112.5GM/50ML

18 215MG/ML

19 1160MG/ML

20 41MG/ML

21 62%

22 32.5MG/ML

23 120%

24 120,000 UNITS/ML

25 1200MG/ML

26 1200MG/VIAL

27 220MG/ML

28 1234MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

29 1250MG/ML

30 625MG/ML

31 1270MG/30ML (9MG/ML)

32 62MEQ/ML

33 14%

34 240MG/ML

35 25,000 UNITS/ML

36 1500MG/100ML

37 1500MG/ML

38 650MG/ML

39 250MG/VIAL

40 35MG/ML

41 280MG/ML

42 180MG/ML;16MG/ML

43 190MG/10ML (9MG/ML)

44 1EQ 0.004MG CHROMIUM/ML

45 1EQ 0.1MG MANGANESE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

46 1EQ 0.4MG COPPER/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

47 3EQ 100MG BASE/VIAL

48 1EQ 10GM BASE/VIAL

49 1EQ 10MG BASE/ML

50 2EQ 125MG BASE/VIAL

51 1EQ 12MG BASE/ML

52 1EQ 150MG BASE/ML

53 1EQ 1GM BASE/3ML

54 8EQ 1GM BASE/VIAL

55 1EQ 1MG ZINC/ML

56 1EQ 2.5MG BASE/ML

57 2EQ 20GM BASE/VIAL

58 1EQ 20MG BASE/VIAL

59 1EQ 250MG BASE/VIAL

60 2EQ 25MG BASE/ML

61 2EQ 2GM BASE/VIAL

62 2EQ 40MG BASE/VIAL

63 1EQ 4GM BASE/VIAL

64 1EQ 4MG PHOSPHATE/ML

65 1EQ 500MG BASE/2ML

66 8EQ 500MG BASE/VIAL

67 2EQ 50MG BASE/VIAL

68 1EQ 5MG BASE/ML

69 1EQ 75MG BASE/2ML

70 1EQ 900MG BASE/100ML

71 1EQ 90MG CALCIUM/5ML

filter Regulatory Info Reset all filters

140 All

01 139DISCN

02 1RX

List of Suppliers

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01

Brand Name : AMINOCAPROIC ACID

U.S.A

Pharma, Lab & Chemical Expo

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Brand Name : AMINOCAPROIC ACID

U.S.A

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RLD : No

TE Code :

AMINOCAPROIC ACID

ABRAXIS PHARM

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : AMINOCAPROIC ACID

Dosage Strength : 250MG/ML

Approval Date : 1986-06-17

Application Number : 70522

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Product
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02

Brand Name : AMINOPHYLLINE

U.S.A

Pharma, Lab & Chemical Expo

Not Confirmed

Brand Name : AMINOPHYLLINE

U.S.A

Pharma, Lab & Chemical Expo

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RLD : No

TE Code :

AMINOPHYLLINE

ABRAXIS PHARM

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : AMINOPHYLLINE

Dosage Strength : 25MG/ML

Approval Date : 1982-01-01

Application Number : 84568

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Product
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03

Brand Name : AMINOPHYLLINE

U.S.A

Pharma, Lab & Chemical Expo

Not Confirmed

Brand Name : AMINOPHYLLINE

U.S.A

Pharma, Lab & Chemical Expo

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RLD : No

TE Code :

AMINOPHYLLINE

ABRAXIS PHARM

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : AMINOPHYLLINE

Dosage Strength : 25MG/ML

Approval Date : 1982-01-01

Application Number : 87200

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Product
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04

Brand Name : AMINOPHYLLINE

U.S.A

Pharma, Lab & Chemical Expo

Not Confirmed

Brand Name : AMINOPHYLLINE

U.S.A

Pharma, Lab & Chemical Expo

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Digital Content

RLD : No

TE Code :

AMINOPHYLLINE

ABRAXIS PHARM

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : AMINOPHYLLINE

Dosage Strength : 25MG/ML

Approval Date : 1982-01-06

Application Number : 87250

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Product
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05

Brand Name : AMINOPHYLLINE

U.S.A

Pharma, Lab & Chemical Expo

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Brand Name : AMINOPHYLLINE

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Pharma, Lab & Chemical Expo

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RLD : No

TE Code :

AMINOPHYLLINE

ABRAXIS PHARM

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : AMINOPHYLLINE

Dosage Strength : 25MG/ML

Approval Date : 1983-08-30

Application Number : 87886

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Product
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06

Brand Name : AMINOPHYLLINE

U.S.A

Pharma, Lab & Chemical Expo

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Brand Name : AMINOPHYLLINE

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RLD : No

TE Code :

AMINOPHYLLINE

ABRAXIS PHARM

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : AMINOPHYLLINE

Dosage Strength : 25MG/ML

Approval Date : 1984-01-25

Application Number : 88407

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Product
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07

Brand Name : AMPHOTERICIN B

U.S.A

Pharma, Lab & Chemical Expo

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Brand Name : AMPHOTERICIN B

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RLD : No

TE Code :

AMPHOTERICIN B

ABRAXIS PHARM

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : AMPHOTERICIN B

Dosage Strength : 50MG/VIAL

Approval Date : 1987-04-13

Application Number : 62728

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Product
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08

Brand Name : M.V.C. 9+3

U.S.A

Pharma, Lab & Chemical Expo

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Brand Name : M.V.C. 9+3

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Digital Content

RLD : No

TE Code :

ASCORBIC ACID; BIOTIN; CYANOCOBALAMIN; DEXPANTHENOL; ERGOCALCIFEROL; FOLIC ACID; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN 5-PHOSPHATE SODIUM; THIAMINE HYDROCHLORIDE; VITAMIN A; VITAMIN E

ABRAXIS PHARM

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : M.V.C. 9+3

Dosage Strength : 10MG/ML;0.006MG/ML;0.5MC...

Approval Date : 1985-08-08

Application Number : 18440

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Product
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09

Brand Name : BRETYLIUM TOSYLATE

U.S.A

Pharma, Lab & Chemical Expo

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Brand Name : BRETYLIUM TOSYLATE

U.S.A

Pharma, Lab & Chemical Expo

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RLD : No

TE Code :

BRETYLIUM TOSYLATE

ABRAXIS PHARM

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : BRETYLIUM TOSYLATE

Dosage Strength : 50MG/ML

Approval Date : 1986-04-29

Application Number : 70134

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Product
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10

Brand Name : BRETYLIUM TOSYLATE

U.S.A

Pharma, Lab & Chemical Expo

Not Confirmed

Brand Name : BRETYLIUM TOSYLATE

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Pharma, Lab & Chemical Expo

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RLD : No

TE Code :

BRETYLIUM TOSYLATE

ABRAXIS PHARM

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : BRETYLIUM TOSYLATE

Dosage Strength : 100MG/ML

Approval Date : 1987-02-13

Application Number : 71298

RX/OTC/DISCN : DISCN

RLD : No

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