Abic Ltd.
FDA Approved Drugs

Abic Ltd.

FDA Approved Drugs Database

FDA approved drug product records including application numbers, product numbers, drug names, active ingredients, dosage forms, strengths, approval dates and regulatory status.

Discontinued
  • Total Records 8
  • Latest Approval Date Jun 01, 1988
  • Data Source FDA
  • First Approval Date Mar 04, 1986
Company Overview

Company

Abic Ltd.

Country

Israel

Website

Email

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Company Snapshot

Abic Ltd.

Kiryat Sapir Industrial Zone P.O.Box 8077 Netanya, 42504

Israel

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FDA Approved Drug Records ( 8 records )
1987
10 Mar
Discontinued Application: 89161

Drug Name

ABITREXATE

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE/ML

Approval Date

1987-03-10

89161 / 1

Active Ingredient

METHOTREXATE SODIUM

Application Number

89161

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE/ML

Approval Date

1987-03-10

Regulatory Status

Discontinued

1987
17 Jul
Discontinued Application: 89354

Drug Name

ABITREXATE

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE/VIAL

Approval Date

1987-07-17

89354 / 1

Active Ingredient

METHOTREXATE SODIUM

Application Number

89354

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE/VIAL

Approval Date

1987-07-17

Regulatory Status

Discontinued

1987
17 Jul
Discontinued Application: 89355

Drug Name

ABITREXATE

Product Number

1

Dosage Form

-

Strength

EQ 100MG BASE/VIAL

Approval Date

1987-07-17

89355 / 1

Active Ingredient

METHOTREXATE SODIUM

Application Number

89355

Product Number

1

Dosage Form

-

Strength

EQ 100MG BASE/VIAL

Approval Date

1987-07-17

Regulatory Status

Discontinued

1987
17 Jul
Discontinued Application: 89356

Drug Name

ABITREXATE

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE/VIAL

Approval Date

1987-07-17

89356 / 1

Active Ingredient

METHOTREXATE SODIUM

Application Number

89356

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE/VIAL

Approval Date

1987-07-17

Regulatory Status

Discontinued

1986
04 Mar
Discontinued Application: 88929

Drug Name

FLUOROURACIL

Product Number

1

Dosage Form

-

Strength

50MG/ML

Approval Date

1986-03-04

88929 / 1

Active Ingredient

FLUOROURACIL

Application Number

88929

Product Number

1

Dosage Form

-

Strength

50MG/ML

Approval Date

1986-03-04

Regulatory Status

Discontinued

1988
01 Jun
Discontinued Application: 89352

Drug Name

LEUCOVORIN CALCIUM

Product Number

1

Dosage Form

-

Strength

EQ 3MG BASE/ML (EQ 3MG BASE/ML)

Approval Date

1988-06-01

89352 / 1

Active Ingredient

LEUCOVORIN CALCIUM

Application Number

89352

Product Number

1

Dosage Form

-

Strength

EQ 3MG BASE/ML (EQ 3MG BASE/ML)

Approval Date

1988-06-01

Regulatory Status

Discontinued

1988
01 Jun
Discontinued Application: 89353

Drug Name

LEUCOVORIN CALCIUM

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE/VIAL

Approval Date

1988-06-01

89353 / 1

Active Ingredient

LEUCOVORIN CALCIUM

Application Number

89353

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE/VIAL

Approval Date

1988-06-01

Regulatory Status

Discontinued

1987
19 Feb
Discontinued Application: 70873

Drug Name

VINCRISTINE SULFATE

Product Number

1

Dosage Form

-

Strength

1MG/ML

Approval Date

1987-02-19

70873 / 1

Active Ingredient

VINCRISTINE SULFATE

Application Number

70873

Product Number

1

Dosage Form

-

Strength

1MG/ML

Approval Date

1987-02-19

Regulatory Status

Discontinued

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Drug Status Breakdown
8 total
  • Discontinued
Official Source

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Drug Name

ABITREXATE

Application Number

89161

Product Number

1

Active Ingredient

METHOTREXATE SODIUM

Dosage Form

-

Strength

EQ 25MG BASE/ML

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