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Naproxen Sodium
Naproxen Sodium - 62207-750-44 - (Naproxen Sodium)
Drug Information of Naproxen Sodium
| Product NDC: | 62207-750 |
| Proprietary Name: | Naproxen Sodium |
| Non Proprietary Name: | Naproxen Sodium |
| Active Ingredient(s): | 220 mg/1 & nbsp; Naproxen Sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Naproxen Sodium
| Product NDC: | 62207-750 |
| Labeler Name: | Granules India Limited |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA091353 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110930 |
Package Information of Naproxen Sodium
| Package NDC: | 62207-750-44 |
| Package Description: | 150 TABLET in 1 BOTTLE (62207-750-44) |
NDC Information of Naproxen Sodium
| NDC Code | 62207-750-44 |
| Proprietary Name | Naproxen Sodium |
| Package Description | 150 TABLET in 1 BOTTLE (62207-750-44) |
| Product NDC | 62207-750 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Naproxen Sodium |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110930 |
| Marketing Category Name | ANDA |
| Labeler Name | Granules India Limited |
| Substance Name | NAPROXEN SODIUM |
| Strength Number | 220 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
