KYNMOBI
- Product NDC
- 63402-120
- 11-digit product format
- 634020120
- Labeler code
- 63402
- Product ID
- 63402-120_d6c3ecd5-c695-45b9-99c9-8e6a34488cca
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- apomorphine hydrochloride
- Dosage form
- FILM, SOLUBLE
- Route
- SUBLINGUAL
- Labeler
- Sunovion Pharmaceuticals Inc.
- Application
- NDA210875
- Marketing category
- NDA
- Marketing start
- 2020-05-21
- Marketing end
- 0000-00-00
- Substance
- APOMORPHINE HYDROCHLORIDE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Dopamine Agonists [MoA], Dopaminergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 63402-120-30 | 63402012030 | 30 POUCH in 1 CARTON (63402-120-30) > 1 FILM, SOLUBLE in 1 POUCH (63402-120-01) | 30 pouch | 2020-05-21 | 0000-00-00 | Yes | No | Current |