Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations
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Search results from the "OB_Rx" table for query
on "020164."
| Active Ingredient: |
ENOXAPARIN SODIUM |
| Dosage Form;Route: |
INJECTABLE; SUBCUTANEOUS |
| Proprietary Name: |
LOVENOX (PRESERVATIVE FREE) |
| Applicant: |
SANOFI AVENTIS US |
| Strength: |
30MG/0.3ML (100MG/ML) |
| Application Number: |
N020164 |
| Product Number: |
001 |
| Approval Date: |
Mar 29, 1993 |
| Reference Listed Drug |
No |
| RX/OTC/DISCN: |
RX |
| TE Code: |
AP |
| Patent and Exclusivity Info for this product: |
View |
|
| Active Ingredient: |
ENOXAPARIN SODIUM |
| Dosage Form;Route: |
INJECTABLE; SUBCUTANEOUS |
| Proprietary Name: |
LOVENOX (PRESERVATIVE FREE) |
| Applicant: |
SANOFI AVENTIS US |
| Strength: |
40MG/0.4ML (100MG/ML) |
| Application Number: |
N020164 |
| Product Number: |
002 |
| Approval Date: |
Jan 30, 1998 |
| Reference Listed Drug |
No |
| RX/OTC/DISCN: |
RX |
| TE Code: |
AP |
| Patent and Exclusivity Info for this product: |
View |
|
| Active Ingredient: |
ENOXAPARIN SODIUM |
| Dosage Form;Route: |
INJECTABLE; SUBCUTANEOUS |
| Proprietary Name: |
LOVENOX (PRESERVATIVE FREE) |
| Applicant: |
SANOFI AVENTIS US |
| Strength: |
60MG/0.6ML (100MG/ML) |
| Application Number: |
N020164 |
| Product Number: |
003 |
| Approval Date: |
Mar 27, 1998 |
| Reference Listed Drug |
No |
| RX/OTC/DISCN: |
RX |
| TE Code: |
AP |
| Patent and Exclusivity Info for this product: |
View |
|
| Active Ingredient: |
ENOXAPARIN SODIUM |
| Dosage Form;Route: |
INJECTABLE; SUBCUTANEOUS |
| Proprietary Name: |
LOVENOX (PRESERVATIVE FREE) |
| Applicant: |
SANOFI AVENTIS US |
| Strength: |
80MG/0.8ML (100MG/ML) |
| Application Number: |
N020164 |
| Product Number: |
004 |
| Approval Date: |
Mar 27, 1998 |
| Reference Listed Drug |
No |
| RX/OTC/DISCN: |
RX |
| TE Code: |
AP |
| Patent and Exclusivity Info for this product: |
View |
|
| Active Ingredient: |
ENOXAPARIN SODIUM |
| Dosage Form;Route: |
INJECTABLE; SUBCUTANEOUS |
| Proprietary Name: |
LOVENOX (PRESERVATIVE FREE) |
| Applicant: |
SANOFI AVENTIS US |
| Strength: |
100MG/ML (100MG/ML) |
| Application Number: |
N020164 |
| Product Number: |
005 |
| Approval Date: |
Mar 27, 1998 |
| Reference Listed Drug |
Yes |
| RX/OTC/DISCN: |
RX |
| TE Code: |
AP |
| Patent and Exclusivity Info for this product: |
View |
|
| Active Ingredient: |
ENOXAPARIN SODIUM |
| Dosage Form;Route: |
INJECTABLE; SUBCUTANEOUS |
| Proprietary Name: |
LOVENOX (PRESERVATIVE FREE) |
| Applicant: |
SANOFI AVENTIS US |
| Strength: |
120MG/0.8ML (150MG/ML) |
| Application Number: |
N020164 |
| Product Number: |
007 |
| Approval Date: |
Jun 2, 2000 |
| Reference Listed Drug |
No |
| RX/OTC/DISCN: |
RX |
| TE Code: |
AP |
| Patent and Exclusivity Info for this product: |
View |
|
| Active Ingredient: |
ENOXAPARIN SODIUM |
| Dosage Form;Route: |
INJECTABLE; SUBCUTANEOUS |
| Proprietary Name: |
LOVENOX (PRESERVATIVE FREE) |
| Applicant: |
SANOFI AVENTIS US |
| Strength: |
150MG/ML (150MG/ML) |
| Application Number: |
N020164 |
| Product Number: |
008 |
| Approval Date: |
Jun 2, 2000 |
| Reference Listed Drug |
No |
| RX/OTC/DISCN: |
RX |
| TE Code: |
AP |
| Patent and Exclusivity Info for this product: |
View |
|
| Active Ingredient: |
ENOXAPARIN SODIUM |
| Dosage Form;Route: |
INJECTABLE; INTRAVENOUS, SUBCUTANEOUS |
| Proprietary Name: |
LOVENOX |
| Applicant: |
SANOFI AVENTIS US |
| Strength: |
300MG/3ML (100MG/ML) |
| Application Number: |
N020164 |
| Product Number: |
009 |
| Approval Date: |
Jan 23, 2003 |
| Reference Listed Drug |
No |
| RX/OTC/DISCN: |
RX |
| TE Code: |
AB |
| Patent and Exclusivity Info for this product: |
View |
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FDA/Center for Drug Evaluation and Research
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Office of Generic Drugs
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Division of Labeling and Program Support
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Update Frequency: |
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Orange Book Data - Monthly
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Generic Drug Product Information & Patent Information - Daily
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Orange Book Data Updated Through April, 2013
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Patent and Generic Drug Product Data Last Updated: May 17, 2013
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