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NAPRELAN
NAPRELAN - 68453-900-02 - (naproxen sodium)
Drug Information of NAPRELAN
| Product NDC: | 68453-900 |
| Proprietary Name: | NAPRELAN |
| Non Proprietary Name: | naproxen sodium |
| Active Ingredient(s): | & nbsp; naproxen sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NAPRELAN
| Product NDC: | 68453-900 |
| Labeler Name: | Victory Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020353 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20091015 |
Package Information of NAPRELAN
| Package NDC: | 68453-900-02 |
| Package Description: | 1 KIT in 1 DOSE PACK (68453-900-02) |
NDC Information of NAPRELAN
| NDC Code | 68453-900-02 |
| Proprietary Name | NAPRELAN |
| Package Description | 1 KIT in 1 DOSE PACK (68453-900-02) |
| Product NDC | 68453-900 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | naproxen sodium |
| Dosage Form Name | KIT |
| Route Name | ORAL |
| Start Marketing Date | 20091015 |
| Marketing Category Name | NDA |
| Labeler Name | Victory Pharma, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
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