PURACAP PHARM
FDA Approved Drugs

PURACAP PHARM

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 RX
  • Total Records 11
  • Latest Approval Date Sep 04, 2007
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
11
View
Discontinued
9
View
RX
2
View
Company Overview

Company

PURACAP PHARM

Country

U.S.A

Website

Visit Website

Email

info@PuraCap.com

Social Profiles

Company Snapshot

PURACAP PHARM

1001 Durham Ave South Plainfield, NJ 07080

U.S.A

puracap.net/  info@PuraCap.com View on Map
FDA Approved Drug Records ( 11 records )
1982
10 Dec
Discontinued Application: 87762

Drug Name

ACETAMINOPHEN AND CODEINE PHOSPHATE

Product Number

1

Dosage Form

-

Strength

300MG;30MG

Approval Date

1982-12-10

87762 / 1

Active Ingredient

ACETAMINOPHEN; CODEINE PHOSPHATE

Application Number

87762

Product Number

1

Dosage Form

-

Strength

300MG;30MG

Approval Date

1982-12-10

Regulatory Status

Discontinued

1985
10 Dec
Discontinued Application: 70147

Drug Name

ALLOPURINOL

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

1985-12-10

70147 / 1

Active Ingredient

ALLOPURINOL

Application Number

70147

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

1985-12-10

Regulatory Status

Discontinued

1985
10 Dec
Discontinued Application: 70150

Drug Name

ALLOPURINOL

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1985-12-10

70150 / 1

Active Ingredient

ALLOPURINOL

Application Number

70150

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1985-12-10

Regulatory Status

Discontinued

2007
04 Sep
Discontinued Application: 78131

Drug Name

AMLODIPINE BESYLATE

Product Number

1

Dosage Form

-

Strength

EQ 2.5MG BASE

Approval Date

2007-09-04

78131 / 1

Active Ingredient

AMLODIPINE BESYLATE

Application Number

78131

Product Number

1

Dosage Form

-

Strength

EQ 2.5MG BASE

Approval Date

2007-09-04

Regulatory Status

Discontinued

2007
04 Sep
Discontinued Application: 78131

Drug Name

AMLODIPINE BESYLATE

Product Number

2

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2007-09-04

78131 / 2

Active Ingredient

AMLODIPINE BESYLATE

Application Number

78131

Product Number

2

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2007-09-04

Regulatory Status

Discontinued

2007
04 Sep
Discontinued Application: 78131

Drug Name

AMLODIPINE BESYLATE

Product Number

3

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2007-09-04

78131 / 3

Active Ingredient

AMLODIPINE BESYLATE

Application Number

78131

Product Number

3

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2007-09-04

Regulatory Status

Discontinued

1983
09 Dec
Discontinued Application: 87048

Drug Name

BUTALBITAL, ASPIRIN AND CAFFEINE

Product Number

2

Dosage Form

-

Strength

325MG;50MG;40MG

Approval Date

1983-12-09

87048 / 2

Active Ingredient

ASPIRIN; BUTALBITAL; CAFFEINE

Application Number

87048

Product Number

2

Dosage Form

-

Strength

325MG;50MG;40MG

Approval Date

1983-12-09

Regulatory Status

Discontinued

2006
19 Jul
RX Application: 77938

Drug Name

MELOXICAM

Product Number

1

Dosage Form

-

Strength

7.5MG

Approval Date

2006-07-19

77938 / 1

Active Ingredient

MELOXICAM

Application Number

77938

Product Number

1

Dosage Form

-

Strength

7.5MG

Approval Date

2006-07-19

Regulatory Status

RX

2006
19 Jul
RX Application: 77938

Drug Name

MELOXICAM

Product Number

2

Dosage Form

-

Strength

15MG

Approval Date

2006-07-19

77938 / 2

Active Ingredient

MELOXICAM

Application Number

77938

Product Number

2

Dosage Form

-

Strength

15MG

Approval Date

2006-07-19

Regulatory Status

RX

1982
01 Jan
Discontinued Application: 84231

Drug Name

METHOCARBAMOL

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

84231 / 2

Active Ingredient

METHOCARBAMOL

Application Number

84231

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84471

Drug Name

METHOCARBAMOL

Product Number

1

Dosage Form

-

Strength

750MG

Approval Date

1982-01-01

84471 / 1

Active Ingredient

METHOCARBAMOL

Application Number

84471

Product Number

1

Dosage Form

-

Strength

750MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

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Drug Status Breakdown
11 total
  • Discontinued
  • 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

ACETAMINOPHEN AND CODEINE PHOSPHATE

Application Number

87762

Product Number

1

Active Ingredient

ACETAMINOPHEN; CODEINE PHOSPHATE

Dosage Form

-

Strength

300MG;30MG

FDA Approved Drug Data

Approved drug product information

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