Zameer Pharmaceuticals
FDA Approved Drugs

Zameer Pharmaceuticals

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.

RX
  • Total Records 10
  • Latest Approval Date Feb 16, 2022
  • Data Source FDA
  • First Approval Date Oct 20, 2021
Company Overview

Company

Zameer Pharmaceuticals

Country

U.S.A

Email

Social Profiles

Company Snapshot

Zameer Pharmaceuticals

33 WOOD AVENUE SUITE 454 ISELIN, NJ 08830

U.S.A

zameerpharma.com/ View on Map
FDA Approved Drug Records ( 10 records )
2021
29 Nov
RX Application: 212630

Drug Name

CHLORPROMAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2021-11-29

212630 / 1

Active Ingredient

CHLORPROMAZINE HYDROCHLORIDE

Application Number

212630

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2021-11-29

Regulatory Status

RX

2021
29 Nov
RX Application: 212630

Drug Name

CHLORPROMAZINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

2021-11-29

212630 / 2

Active Ingredient

CHLORPROMAZINE HYDROCHLORIDE

Application Number

212630

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

2021-11-29

Regulatory Status

RX

2021
29 Nov
RX Application: 212630

Drug Name

CHLORPROMAZINE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

2021-11-29

212630 / 3

Active Ingredient

CHLORPROMAZINE HYDROCHLORIDE

Application Number

212630

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

2021-11-29

Regulatory Status

RX

2021
29 Nov
RX Application: 212630

Drug Name

CHLORPROMAZINE HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

100MG

Approval Date

2021-11-29

212630 / 4

Active Ingredient

CHLORPROMAZINE HYDROCHLORIDE

Application Number

212630

Product Number

4

Dosage Form

-

Strength

100MG

Approval Date

2021-11-29

Regulatory Status

RX

2021
29 Nov
RX Application: 212630

Drug Name

CHLORPROMAZINE HYDROCHLORIDE

Product Number

5

Dosage Form

-

Strength

200MG

Approval Date

2021-11-29

212630 / 5

Active Ingredient

CHLORPROMAZINE HYDROCHLORIDE

Application Number

212630

Product Number

5

Dosage Form

-

Strength

200MG

Approval Date

2021-11-29

Regulatory Status

RX

2021
20 Oct
RX Application: 215141

Drug Name

FLUPHENAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

2021-10-20

215141 / 1

Active Ingredient

FLUPHENAZINE HYDROCHLORIDE

Application Number

215141

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

2021-10-20

Regulatory Status

RX

2021
20 Oct
RX Application: 215141

Drug Name

FLUPHENAZINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

2.5MG

Approval Date

2021-10-20

215141 / 2

Active Ingredient

FLUPHENAZINE HYDROCHLORIDE

Application Number

215141

Product Number

2

Dosage Form

-

Strength

2.5MG

Approval Date

2021-10-20

Regulatory Status

RX

2021
20 Oct
RX Application: 215141

Drug Name

FLUPHENAZINE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

5MG

Approval Date

2021-10-20

215141 / 3

Active Ingredient

FLUPHENAZINE HYDROCHLORIDE

Application Number

215141

Product Number

3

Dosage Form

-

Strength

5MG

Approval Date

2021-10-20

Regulatory Status

RX

2021
20 Oct
RX Application: 215141

Drug Name

FLUPHENAZINE HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

10MG

Approval Date

2021-10-20

215141 / 4

Active Ingredient

FLUPHENAZINE HYDROCHLORIDE

Application Number

215141

Product Number

4

Dosage Form

-

Strength

10MG

Approval Date

2021-10-20

Regulatory Status

RX

2022
16 Feb
RX Application: 215781

Drug Name

TROSPIUM CHLORIDE

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

2022-02-16

215781 / 1

Active Ingredient

TROSPIUM CHLORIDE

Application Number

215781

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

2022-02-16

Regulatory Status

RX

Related Databases
  • FDA Inspections
    0 View
  • EDQM CEP
    0 View
  • KDMF
    0 View
  • Japan DMF
    0 View
  • Eudra GMP
    0 View
  • NDC Database
    0 View
  • FDA Approved Drugs Database
    10 View
  • Drug Prices in Switzerland
    0 View
Drug Status Breakdown
10 total
  • RX
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

CHLORPROMAZINE HYDROCHLORIDE

Application Number

212630

Product Number

1

Active Ingredient

CHLORPROMAZINE HYDROCHLORIDE

Dosage Form

-

Strength

10MG

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

Create a New Buying Request

Fields marked with * are mandatory.

Please enter quantity.
Please select a unit.
Please select quality standard.
Please select request type.
Please provide product specifications.
Please enter additional details.
Please select shipping preference.
Notice: By submitting this buying request, the provided product details and requirements may be published publicly on our marketplace.