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Seromycin
Seromycin - 49349-018-02 - (CYCLOSERINE)
Drug Information of Seromycin
| Product NDC: | 49349-018 |
| Proprietary Name: | Seromycin |
| Non Proprietary Name: | CYCLOSERINE |
| Active Ingredient(s): | 250 mg/1 & nbsp; CYCLOSERINE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Seromycin
| Product NDC: | 49349-018 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA060593 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110802 |
Package Information of Seromycin
| Package NDC: | 49349-018-02 |
| Package Description: | 30 CAPSULE in 1 BLISTER PACK (49349-018-02) |
NDC Information of Seromycin
| NDC Code | 49349-018-02 |
| Proprietary Name | Seromycin |
| Package Description | 30 CAPSULE in 1 BLISTER PACK (49349-018-02) |
| Product NDC | 49349-018 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CYCLOSERINE |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20110802 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | CYCLOSERINE |
| Strength Number | 250 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
