Novast Laboratories Unclassified
FDA Approved Drugs

Novast Laboratories 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 14
  • Latest Approval Date -
  • Data Source FDA
  • First Approval Date -
All
94
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Unclassified
14
View
OTC
1
View
RX
79
View
Company Overview

Company

Novast Laboratories Unclassified

Country

China

Website

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Company Snapshot

Novast Laboratories Unclassified

1692 Xinghu Road, Suite A-3, Bldg 21, Jiangsu Prov.,, Nantong, Jiangsu 226009

China

www.novastlabs.com/ View on Map
FDA Approved Drug Records ( 14 records )
-
Unclassified Application: 91690

Drug Name

ETHINYL ESTRADIOL AND LEVONORGESTREL

Product Number

1

Dosage Form

-

Strength

0.03MG,0.01MG; 0.15MG,N/A

Approval Date

-

91690 / 1

Active Ingredient

ETHINYL ESTRADIOL; LEVONORGESTREL

Application Number

91690

Product Number

1

Dosage Form

-

Strength

0.03MG,0.01MG; 0.15MG,N/A

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 208661

Drug Name

LO LARIN FE

Product Number

1

Dosage Form

-

Strength

0.01MG,0.01MG;1MG,N/A

Approval Date

-

208661 / 1

Active Ingredient

ETHINYL ESTRADIOL; NORETHINDRONE ACETATE

Application Number

208661

Product Number

1

Dosage Form

-

Strength

0.01MG,0.01MG;1MG,N/A

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 214731

Drug Name

MEMANTINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

7MG

Approval Date

-

214731 / 1

Active Ingredient

MEMANTINE HYDROCHLORIDE

Application Number

214731

Product Number

1

Dosage Form

-

Strength

7MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 214731

Drug Name

MEMANTINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

14MG

Approval Date

-

214731 / 2

Active Ingredient

MEMANTINE HYDROCHLORIDE

Application Number

214731

Product Number

2

Dosage Form

-

Strength

14MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 214731

Drug Name

MEMANTINE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

21MG

Approval Date

-

214731 / 3

Active Ingredient

MEMANTINE HYDROCHLORIDE

Application Number

214731

Product Number

3

Dosage Form

-

Strength

21MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 214731

Drug Name

MEMANTINE HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

28MG

Approval Date

-

214731 / 4

Active Ingredient

MEMANTINE HYDROCHLORIDE

Application Number

214731

Product Number

4

Dosage Form

-

Strength

28MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 218724

Drug Name

OXCARBAZEPINE

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

-

218724 / 2

Active Ingredient

OXCARBAZEPINE

Application Number

218724

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 218724

Drug Name

OXCARBAZEPINE

Product Number

3

Dosage Form

-

Strength

600MG

Approval Date

-

218724 / 3

Active Ingredient

OXCARBAZEPINE

Application Number

218724

Product Number

3

Dosage Form

-

Strength

600MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 218069

Drug Name

SITAGLIPTIN AND METFORMIN HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 100MG BASE TABLET

Approval Date

-

218069 / 2

Active Ingredient

METFORMIN HYDROCHLORIDE, SITAGLIPTIN

Application Number

218069

Product Number

2

Dosage Form

-

Strength

EQ 100MG BASE TABLET

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 218069

Drug Name

SITAGLIPTIN AND METFORMIN HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

500MG

Approval Date

-

218069 / 3

Active Ingredient

METFORMIN HYDROCHLORIDE, SITAGLIPTIN

Application Number

218069

Product Number

3

Dosage Form

-

Strength

500MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 218069

Drug Name

SITAGLIPTIN AND METFORMIN HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

50MG

Approval Date

-

218069 / 4

Active Ingredient

METFORMIN HYDROCHLORIDE, SITAGLIPTIN

Application Number

218069

Product Number

4

Dosage Form

-

Strength

50MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 218069

Drug Name

SITAGLIPTIN AND METFORMIN HYDROCHLORIDE

Product Number

5

Dosage Form

-

Strength

1000MG

Approval Date

-

218069 / 5

Active Ingredient

METFORMIN HYDROCHLORIDE, SITAGLIPTIN

Application Number

218069

Product Number

5

Dosage Form

-

Strength

1000MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 90541

Drug Name

TRI-LO-LINYAH

Product Number

2

Dosage Form

-

Strength

0.215MG; 0.025MG

Approval Date

-

90541 / 2

Active Ingredient

NORGESTIMATE; ETHINYL ESTRADIOL

Application Number

90541

Product Number

2

Dosage Form

-

Strength

0.215MG; 0.025MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 90541

Drug Name

TRI-LO-LINYAH

Product Number

3

Dosage Form

-

Strength

0.25MG; 0.025MG

Approval Date

-

90541 / 3

Active Ingredient

NORGESTIMATE; ETHINYL ESTRADIOL

Application Number

90541

Product Number

3

Dosage Form

-

Strength

0.25MG; 0.025MG

Approval Date

-

Regulatory Status

Unclassified

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Drug Status Breakdown
14 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

ETHINYL ESTRADIOL AND LEVONORGESTREL

Application Number

91690

Product Number

1

Active Ingredient

ETHINYL ESTRADIOL; LEVONORGESTREL

Dosage Form

-

Strength

0.03MG,0.01MG; 0.15MG,N/A

FDA Approved Drug Data

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