Sernivo
- Product NDC
- 69482-800
- 11-digit product format
- 694820800
- Labeler code
- 69482
- Product ID
- 69482-800_93683e1f-f5bc-47e4-b1af-e1755279451e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- betamethasone dipropionate
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Encore Dermatology Inc.
- Application
- NDA208079
- Marketing category
- NDA
- Marketing start
- 2020-01-01
- Marketing end
- 0000-00-00
- Substance
- BETAMETHASONE DIPROPIONATE
- Active strength
- 1 mg/g
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69482-800-99 | 69482080099 | 1 BOTTLE, SPRAY in 1 CARTON (69482-800-99) > 120 g in 1 BOTTLE, SPRAY | 2020-01-01 | 0000-00-00 | No | No | Current |