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Plan B
Plan B - 54868-4894-0 - (Levonorgestrel)
Drug Information of Plan B
| Product NDC: | 54868-4894 |
| Proprietary Name: | Plan B |
| Non Proprietary Name: | Levonorgestrel |
| Active Ingredient(s): | .75 mg/1 & nbsp; Levonorgestrel |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Plan B
| Product NDC: | 54868-4894 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021045 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20030814 |
Package Information of Plan B
| Package NDC: | 54868-4894-0 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (54868-4894-0) > 2 TABLET in 1 BLISTER PACK |
NDC Information of Plan B
| NDC Code | 54868-4894-0 |
| Proprietary Name | Plan B |
| Package Description | 1 BLISTER PACK in 1 CARTON (54868-4894-0) > 2 TABLET in 1 BLISTER PACK |
| Product NDC | 54868-4894 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Levonorgestrel |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20030814 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | LEVONORGESTREL |
| Strength Number | .75 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Inhibit Ovum Fertilization [PE],Progesterone Congeners [Chemical/Ingredient],Progesterone Congeners [Chemical/Ingredient],Progestin [EPC],Progestin-containing Intrauterine Device [EPC] |
