Hikma Pharmaceuticals Unclassified
FDA Approved Drugs

Hikma Pharmaceuticals Unclassified

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.

Unclassified
  • Total Records 29
  • Latest Approval Date -
  • Data Source FDA
  • First Approval Date -
All
1144
View
Unclassified
29
View
Discontinued
529
View
OTC
1
View
RX
585
View
Company Overview

Company

Hikma Pharmaceuticals Unclassified

Country

United Kingdom

Website

Visit Website

Email

Sarrar@hikma.com

Social Profiles

LinkedIn X / Twitter
Company Snapshot

Hikma Pharmaceuticals Unclassified

1 New Burlington Place, Mayfair, London, W1S 2HR

United Kingdom

www.hikma.com/home/ Sarrar@hikma.com View on Map
FDA Approved Drug Records ( 29 records )
-
Unclassified Application: 65048

Drug Name

CEFUROXIME

Product Number

3

Dosage Form

-

Strength

1.5G/20ML

Approval Date

-

65048 / 3

Active Ingredient

CEFUROXIME

Application Number

65048

Product Number

3

Dosage Form

-

Strength

1.5G/20ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 65048

Drug Name

CEFUROXIME

Product Number

4

Dosage Form

-

Strength

1.5G/100ML

Approval Date

-

65048 / 4

Active Ingredient

CEFUROXIME

Application Number

65048

Product Number

4

Dosage Form

-

Strength

1.5G/100ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 88557

Drug Name

CHLOROTHIAZIDE AND RESERPINE

Product Number

1

Dosage Form

-

Strength

250MG;0.125MG

Approval Date

-

88557 / 1

Active Ingredient

CHLOROTHIAZIDE; RESERPINE

Application Number

88557

Product Number

1

Dosage Form

-

Strength

250MG;0.125MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 76558

Drug Name

CIPROFLOXACIN

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

-

76558 / 1

Active Ingredient

CIPROFLOXACIN

Application Number

76558

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 88316

Drug Name

DEXAMETHASONE

Product Number

1

Dosage Form

-

Strength

6MG

Approval Date

-

88316 / 1

Active Ingredient

DEXAMETHASONE

Application Number

88316

Product Number

1

Dosage Form

-

Strength

6MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 202651

Drug Name

DILTIAZEM HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

50MG/10ML

Approval Date

-

202651 / 2

Active Ingredient

DILTIAZEM HYDROCHLORIDE

Application Number

202651

Product Number

2

Dosage Form

-

Strength

50MG/10ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 202651

Drug Name

DILTIAZEM HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

125MG/25ML

Approval Date

-

202651 / 3

Active Ingredient

DILTIAZEM HYDROCHLORIDE

Application Number

202651

Product Number

3

Dosage Form

-

Strength

125MG/25ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 215508

Drug Name

EDARAVONE

Product Number

2

Dosage Form

-

Strength

60mg/100mL

Approval Date

-

215508 / 2

Active Ingredient

EDARAVONE

Application Number

215508

Product Number

2

Dosage Form

-

Strength

60mg/100mL

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 761439

Drug Name

ENOBY

Product Number

1

Dosage Form

-

Strength

60MG/ML

Approval Date

-

761439 / 1

Active Ingredient

DENOSUMAB-QBDE

Application Number

761439

Product Number

1

Dosage Form

-

Strength

60MG/ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 218731

Drug Name

ENZALUTAMIDE

Product Number

1

Dosage Form

-

Strength

40MG

Approval Date

-

218731 / 1

Active Ingredient

ENZALUTAMIDE

Application Number

218731

Product Number

1

Dosage Form

-

Strength

40MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 218731

Drug Name

ENZALUTAMIDE

Product Number

2

Dosage Form

-

Strength

80MG

Approval Date

-

218731 / 2

Active Ingredient

ENZALUTAMIDE

Application Number

218731

Product Number

2

Dosage Form

-

Strength

80MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 71107

Drug Name

FLURAZEPAM HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

-

71107 / 1

Active Ingredient

FLURAZEPAM HYDROCHLORIDE

Application Number

71107

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 17007

Drug Name

HEPARIN LOCK FLUSH

Product Number

8

Dosage Form

-

Strength

10 UNITS/ML

Approval Date

-

17007 / 8

Active Ingredient

HEPARIN SODIUM

Application Number

17007

Product Number

8

Dosage Form

-

Strength

10 UNITS/ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 17007

Drug Name

HEPARIN LOCK FLUSH

Product Number

9

Dosage Form

-

Strength

100 UNITS/ML

Approval Date

-

17007 / 9

Active Ingredient

HEPARIN SODIUM

Application Number

17007

Product Number

9

Dosage Form

-

Strength

100 UNITS/ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 87425

Drug Name

ISONIAZID

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

-

87425 / 1

Active Ingredient

ISONIAZID

Application Number

87425

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 75772

Drug Name

KETOROLAC TROMETHAMINE

Product Number

3

Dosage Form

-

Strength

60MG/2ML

Approval Date

-

75772 / 3

Active Ingredient

KETOROLAC TROMETHAMINE

Application Number

75772

Product Number

3

Dosage Form

-

Strength

60MG/2ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 78767

Drug Name

LEVOFLOXACIN

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

-

78767 / 1

Active Ingredient

LEVOFLOXACIN

Application Number

78767

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 78767

Drug Name

LEVOFLOXACIN

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

-

78767 / 2

Active Ingredient

LEVOFLOXACIN

Application Number

78767

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 78767

Drug Name

LEVOFLOXACIN

Product Number

3

Dosage Form

-

Strength

750MG

Approval Date

-

78767 / 3

Active Ingredient

LEVOFLOXACIN

Application Number

78767

Product Number

3

Dosage Form

-

Strength

750MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 75739

Drug Name

MESNA

Product Number

2

Dosage Form

-

Strength

1G/10ML

Approval Date

-

75739 / 2

Active Ingredient

MESNA

Application Number

75739

Product Number

2

Dosage Form

-

Strength

1G/10ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 85159

Drug Name

METHOCARBAMOL

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

-

85159 / 1

Active Ingredient

METHOCARBAMOL

Application Number

85159

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 75660

Drug Name

MILRINONE LACTATE

Product Number

2

Dosage Form

-

Strength

EQ 20MG /20ML (1MG/ML)

Approval Date

-

75660 / 2

Active Ingredient

MILRINONE LACTATE

Application Number

75660

Product Number

2

Dosage Form

-

Strength

EQ 20MG /20ML (1MG/ML)

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 75660

Drug Name

MILRINONE LACTATE

Product Number

3

Dosage Form

-

Strength

EQ 50MG /50ML (1MG/ML)

Approval Date

-

75660 / 3

Active Ingredient

MILRINONE LACTATE

Application Number

75660

Product Number

3

Dosage Form

-

Strength

EQ 50MG /50ML (1MG/ML)

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 78658

Drug Name

ROSIGLITAZONE MALEATE

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

-

78658 / 1

Active Ingredient

ROSIGLITAZONE MALEATE

Application Number

78658

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 78658

Drug Name

ROSIGLITAZONE MALEATE

Product Number

2

Dosage Form

-

Strength

4MG

Approval Date

-

78658 / 2

Active Ingredient

ROSIGLITAZONE MALEATE

Application Number

78658

Product Number

2

Dosage Form

-

Strength

4MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 78658

Drug Name

ROSIGLITAZONE MALEATE

Product Number

3

Dosage Form

-

Strength

8MG

Approval Date

-

78658 / 3

Active Ingredient

ROSIGLITAZONE MALEATE

Application Number

78658

Product Number

3

Dosage Form

-

Strength

8MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 207583

Drug Name

TESTOSTERONE UNDECANOATE

Product Number

1

Dosage Form

-

Strength

750MG/3ML (250MG/ML)

Approval Date

-

207583 / 1

Active Ingredient

TESTOSTERONE UNDECANOATE

Application Number

207583

Product Number

1

Dosage Form

-

Strength

750MG/3ML (250MG/ML)

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 208562

Drug Name

VORICONAZOLE

Product Number

2

Dosage Form

-

Strength

200MG

Approval Date

-

208562 / 2

Active Ingredient

VORICONAZOLE

Application Number

208562

Product Number

2

Dosage Form

-

Strength

200MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 761439

Drug Name

XTRENBO

Product Number

2

Dosage Form

-

Strength

120MG/1.7ML(70MG/ML)

Approval Date

-

761439 / 2

Active Ingredient

DENOSUMAB-QBDE

Application Number

761439

Product Number

2

Dosage Form

-

Strength

120MG/1.7ML(70MG/ML)

Approval Date

-

Regulatory Status

Unclassified

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Drug Status Breakdown
29 total
  • Unclassified
Official Source

FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.

Visit FDA Orange Book
FDA Approved Drug Record Details Preview

Explore important FDA approved drug information available in the records above.

Drug Name

CEFUROXIME

Application Number

65048

Product Number

3

Active Ingredient

CEFUROXIME

Dosage Form

-

Strength

1.5G/20ML

FDA Approved Drug Data

Approved drug product information

Regular Updates

Data maintained from official sources

Structured Database

Searchable pharmaceutical data

Reliable Data

Organized FDA drug records

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