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Meclofenamate Sodium
Meclofenamate Sodium - 0378-3000-05 - (meclofenamate sodium)
Drug Information of Meclofenamate Sodium
| Product NDC: | 0378-3000 |
| Proprietary Name: | Meclofenamate Sodium |
| Non Proprietary Name: | meclofenamate sodium |
| Active Ingredient(s): | 100 mg/1 & nbsp; meclofenamate sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Meclofenamate Sodium
| Product NDC: | 0378-3000 |
| Labeler Name: | Mylan Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA071081 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121009 |
Package Information of Meclofenamate Sodium
| Package NDC: | 0378-3000-05 |
| Package Description: | 500 CAPSULE in 1 BOTTLE (0378-3000-05) |
NDC Information of Meclofenamate Sodium
| NDC Code | 0378-3000-05 |
| Proprietary Name | Meclofenamate Sodium |
| Package Description | 500 CAPSULE in 1 BOTTLE (0378-3000-05) |
| Product NDC | 0378-3000 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | meclofenamate sodium |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20121009 |
| Marketing Category Name | ANDA |
| Labeler Name | Mylan Pharmaceuticals Inc. |
| Substance Name | MECLOFENAMATE SODIUM |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
