NDC 78206-145

Nexplanon

Etonogestrel

Nexplanon is a Subcutaneous Implant in the Human Prescription Drug category. It is labeled and distributed by Organon Llc. The primary component is Etonogestrel.

• Product ID: 78206-145_2b6805f7-1ff5-40bf-a028-a173a7fdb580
• NDC: 78206-145
• Product Type: Human Prescription Drug
• Proprietary Name: Nexplanon
• Generic Name: Etonogestrel
• Dosage Form: Implant
• Route of Administration: SUBCUTANEOUS
• Marketing Start Date: 2021-06-01
• Marketing Category: NDA /
• Application Number: NDA021529
• Labeler Name: Organon LLC
• Substance Name: ETONOGESTREL
• Active Ingredient Strength: 68 mg/1
• Pharm Classes: Progesterone Congeners [CS],Progestin [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2022-12-31

Packaging

NDC 78206-145-01

1 BLISTER PACK in 1 CARTON (78206-145-01) > 1 IMPLANT in 1 BLISTER PACK

• Marketing Start Date: 2021-06-01
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "Nexplanon" or generic name "Etonogestrel"

NDC	Brand Name	Generic Name
0052-4330	Nexplanon	etonogestrel
78206-145	Nexplanon	etonogestrel
0052-0272	IMPLANON	etonogestrel