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01 2ABRAXIS PHARM

02 6Actavis Inc

03 1American Regent

04 1Aneta Pharmaceuticals

05 2Brooks laboratories Limited

06 1Epic Pharma. LLC.

07 3Ind Swift Laboratories Limited

08 1Modern Laboratories

09 17Montage Laboratories

10 1Pluviaendo

11 3Quad Pharma

12 3Woodward Pharma Services

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PharmaCompass

01

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

NANDROLONE DECANOATE

Brand Name : NANDROLONE DECANOATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 100MG/ML

Packaging :

Approval Date : 1983-10-03

Application Number : 88290

Regulatory Info : DISCN

Registration Country : USA

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02

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

NANDROLONE DECANOATE

Brand Name : NANDROLONE DECANOATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 200MG/ML

Packaging :

Approval Date : 1983-10-14

Application Number : 88317

Regulatory Info : DISCN

Registration Country : USA

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03

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

NANDROLONE DECANOATE

Brand Name : NANDROLONE DECANOATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 50MG/ML

Packaging :

Approval Date : 1984-01-13

Application Number : 86385

Regulatory Info : DISCN

Registration Country : USA

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04

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

NANDROLONE DECANOATE

Brand Name : NANDROLONE DECANOATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 100MG/ML

Packaging :

Approval Date : 1984-01-13

Application Number : 86598

Regulatory Info : DISCN

Registration Country : USA

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05

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

NANDROLONE DECANOATE

Brand Name : NANDROLONE DECANOATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 50MG/ML

Packaging :

Approval Date : 1983-10-06

Application Number : 87598

Regulatory Info : DISCN

Registration Country : USA

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06

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

NANDROLONE DECANOATE

Brand Name : NANDROLONE DECANOATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 100MG/ML

Packaging :

Approval Date : 1983-10-06

Application Number : 87599

Regulatory Info : DISCN

Registration Country : USA

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07

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

NANDROLONE DECANOATE

Brand Name : NANDROLONE DECANOATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 200MG/ML

Packaging :

Approval Date : 1983-12-05

Application Number : 88128

Regulatory Info : DISCN

Registration Country : USA

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08

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

NANDROLONE DECANOATE

Brand Name : NANDROLONE DECANOATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 50MG/ML

Packaging :

Approval Date : 1986-02-10

Application Number : 88554

Regulatory Info : DISCN

Registration Country : USA

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09

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

NANDROLONE DECANOATE

Brand Name : NANDROLONE DECANOATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 200MG/ML

Packaging :

Approval Date : 2010-08-30

Application Number : 91252

Regulatory Info : DISCN

Registration Country : USA

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10

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

Nandrolone Decanoate

Brand Name :

Dosage Form : Injection

Dosage Strength : 25MG/ML

Packaging : Ampoule

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

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11

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

NANDROLONE DECANOATE

Brand Name : NANDROLONE DECANOATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 100MG/ML

Packaging :

Approval Date : 1983-09-28

Application Number : 87519

Regulatory Info : DISCN

Registration Country : USA

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12

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

Nandrolone Decanoate

Brand Name :

Dosage Form : INJECTION

Dosage Strength : 100MG

Packaging :

Approval Date :

Application Number : 87519

Regulatory Info : Generic

Registration Country : India

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13

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

Nandrolone Decanoate

Brand Name :

Dosage Form : INJECTION

Dosage Strength : 50MG

Packaging :

Approval Date :

Application Number : 86385

Regulatory Info : Generic

Registration Country : India

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14

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

Nandrolone Decanoate

Brand Name :

Dosage Form : INJECTION

Dosage Strength : 25MG

Packaging :

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : India

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15

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

NANDROLONE DECANOATE

Brand Name : NANDROLONE DECANOATE

Dosage Form : Injectable; Injection

Dosage Strength : 50MG/ML

Packaging :

Approval Date :

Application Number : 89248

Regulatory Info :

Registration Country : USA

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16

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

NANDROLONE DECANOATE

Brand Name : NANDROLONE DECANOATE

Dosage Form : Injectable; Injection

Dosage Strength : 100MG/ML

Packaging :

Approval Date :

Application Number : 89249

Regulatory Info :

Registration Country : USA

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17

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

NANDROLONE DECANOATE

Brand Name : NANDROLONE DECANOATE

Dosage Form : Injectable; Injection

Dosage Strength : 200MG/ML

Packaging :

Approval Date :

Application Number : 89250

Regulatory Info :

Registration Country : USA

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18

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

NANDROLONE DECANOATE

Brand Name : DECA-DURABOLIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 50MG/ML

Packaging :

Approval Date : 1986-06-12

Application Number : 13132

Regulatory Info : DISCN

Registration Country : USA

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19

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

NANDROLONE DECANOATE

Brand Name : DECA-DURABOLIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 100MG/ML

Packaging :

Approval Date : 1986-06-12

Application Number : 13132

Regulatory Info : DISCN

Registration Country : USA

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20

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

NANDROLONE DECANOATE

Brand Name : DECA-DURABOLIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 200MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1986-06-12

Application Number : 13132

Regulatory Info : DISCN

Registration Country : USA

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