Nexplanon
- Product NDC
- 0052-4330
- 11-digit product format
- 000524330
- Labeler code
- 0052
- Product ID
- 0052-4330_275103d5-5887-4cbe-a83e-d6cc11f46732
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- etonogestrel
- Dosage form
- IMPLANT
- Route
- SUBCUTANEOUS
- Labeler
- Organon USA Inc.
- Application
- NDA021529
- Marketing category
- NDA
- Marketing start
- 2013-09-27
- Marketing end
- 0000-00-00
- Substance
- ETONOGESTREL
- Active strength
- 68 mg/1
- Pharmacologic classes
- Progesterone Congeners [CS],Progestin [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0052-4330-01 | 00052433001 | 1 BLISTER PACK in 1 CARTON (0052-4330-01) > 1 IMPLANT in 1 BLISTER PACK | 1 blister pack | 2013-09-27 | 0000-00-00 | No | No | Current |