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Nexplanon
Nexplanon - 0052-0274-01 - (etonogestrel)
Drug Information of Nexplanon
| Product NDC: | 0052-0274 |
| Proprietary Name: | Nexplanon |
| Non Proprietary Name: | etonogestrel |
| Active Ingredient(s): | 68 mg/1 & nbsp; etonogestrel |
| Administration Route(s): | SUBCUTANEOUS |
| Dosage Form(s): | IMPLANT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nexplanon
| Product NDC: | 0052-0274 |
| Labeler Name: | Organon Pharmaceuticals USA |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021529 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20060717 |
Package Information of Nexplanon
| Package NDC: | 0052-0274-01 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (0052-0274-01) > 1 IMPLANT in 1 BLISTER PACK |
NDC Information of Nexplanon
| NDC Code | 0052-0274-01 |
| Proprietary Name | Nexplanon |
| Package Description | 1 BLISTER PACK in 1 CARTON (0052-0274-01) > 1 IMPLANT in 1 BLISTER PACK |
| Product NDC | 0052-0274 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | etonogestrel |
| Dosage Form Name | IMPLANT |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 20060717 |
| Marketing Category Name | NDA |
| Labeler Name | Organon Pharmaceuticals USA |
| Substance Name | ETONOGESTREL |
| Strength Number | 68 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Progesterone Congeners [Chemical/Ingredient],Progestin [EPC] |
