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Approved Drug Products containing 01769_FLUKA listed in the FDA Orange Book. Original Data : FDA Website

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01 1MISSION PHARMA

02 1ABRAXIS PHARM

03 1AMNEAL PHARM

04 1ATHEM

05 1BARR

06 1BEN VENUE

07 1CADILA PHARMS LTD

08 1CHARTWELL MOLECULAR

09 1CONTRACT PHARMACAL

10 1ENDO OPERATIONS

11 1EVERYLIFE

12 1FRESENIUS KABI USA

13 1HALSEY

14 1HIKMA PHARMS

15 7HOSPIRA

16 1IMPAX LABS

17 1IVAX SUB TEVA PHARMS

18 1JUBILANT CADISTA

19 1LANNETT

20 1LEADING

21 1LEDERLE

22 1LILLY

23 1MK LABS

24 1NEXGEN PHARMA INC

25 1NUVO PHARMS INC

26 1PHARMERAL

27 1PIONEER PHARMS

28 1PUREPAC PHARM

29 1QINGDAO BAHEAL PHARM

30 1ROCHE

31 1SANDOZ

32 4SANDOZ CANADA INC

33 1SUN PHARM INDUSTRIES

34 1TABLICAPS

35 1TELIGENT

36 1UDL

37 1USL PHARMA

38 1VALEANT PHARM INTL

39 1VANGARD

40 1VINTAGE PHARMS

41 4WATSON LABS

42 1WHITEWORTH TOWN PLSN

43 2WYETH PHARMS INC

44 1XGEN PHARMS

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PharmaCompass

01

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AAPS 2024
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothMission CDMO team brings reliability, resourcefulness, & responsiveness in executing your development project.

RLD : No

TE Code :

FOLIC ACID

Brand Name : FOLICET

Dosage Form : TABLET;ORAL

Dosage Strength : 1MG

Approval Date : 1982-01-01

Application Number : 87438

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Mission Pharmacal

02

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

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

Brand Name : MVC PLUS

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 10MG/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

Approval Date : 1985-08-08

Application Number : 18439

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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03

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

FOLIC ACID

Brand Name : FOLIC ACID

Dosage Form : TABLET;ORAL

Dosage Strength : 1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 6135

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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04

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

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

Brand Name : BEROCCA PN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 50MG/ML;0.03MG/ML;0.0025MG/ML;7.5MG/ML;100 IU/ML;0.2MG/ML;20MG/ML;2MG/ML;1.8MG/ML;1.5MG/ML;1,650 IU/ML;5 IU/ML

Approval Date : 1985-10-10

Application Number : 6071

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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05

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

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

Brand Name : M.V.I.-12 ADULT

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 10MG/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

Approval Date : 1985-08-08

Application Number : 8809

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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06

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

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

Brand Name : M.V.I.-12 ADULT

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 20MG/ML;0.006MG/ML;0.5MCG/ML;1.5MG/ML;20 IU/ML;0.6MG/ML;4MG/ML;0.4MG/ML;0.36MG/ML;0.6MG/ML;330 UNITS/ML;1 IU/ML

Approval Date : 2004-04-22

Application Number : 8809

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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07

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

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

Brand Name : M.V.I.-12 ADULT

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 20MG/ML;0.006MG/ML;0.05MCG/ML;1.5MG/ML;0.0005MG/ML;0.06MG/ML;4MG/ML;0.6MG/ML;0.36MG/ML;0.6MG/ML;0.1MG/ML;1MG/ML

Approval Date : 2004-09-09

Application Number : 8809

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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08

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

FERROUS SULFATE; FOLIC ACID

Brand Name : FOLVRON

Dosage Form : CAPSULE;ORAL

Dosage Strength : 182MG;0.33MG

Approval Date : 1982-01-01

Application Number : 6012

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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09

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

FOLIC ACID

Brand Name : FOLVITE

Dosage Form : TABLET;ORAL

Dosage Strength : 1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 5897

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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10

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

FOLIC ACID

Brand Name : FOLVITE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 5MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 5897

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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