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Griseofulvin
Griseofulvin - 68682-520-01 - (Griseofulvin)
Drug Information of Griseofulvin
| Product NDC: | 68682-520 |
| Proprietary Name: | Griseofulvin |
| Non Proprietary Name: | Griseofulvin |
| Active Ingredient(s): | 250 mg/1 & nbsp; Griseofulvin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Griseofulvin
| Product NDC: | 68682-520 |
| Labeler Name: | Oceanside Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050475 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20121203 |
Package Information of Griseofulvin
| Package NDC: | 68682-520-01 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68682-520-01) |
NDC Information of Griseofulvin
| NDC Code | 68682-520-01 |
| Proprietary Name | Griseofulvin |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68682-520-01) |
| Product NDC | 68682-520 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Griseofulvin |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20121203 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Oceanside Pharmaceuticals |
| Substance Name | GRISEOFULVIN |
| Strength Number | 250 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Decreased Mitosis [PE],Microtubule Inhibition [PE],Tubulin Inhibiting Agent [EPC] |
