Mometasone Furoate Monohydrate
- Product NDC
- 0781-6355
- 11-digit product format
- 007816355
- Labeler code
- 0781
- Product ID
- 0781-6355_74bb6412-7e0d-46ad-bbf6-26aa7e5d6c04
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mometasone Furoate Monohydrate
- Dosage form
- SPRAY, METERED
- Route
- NASAL
- Labeler
- Sandoz Inc.
- Application
- NDA020762
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2016-03-25
- Marketing end
- 2021-10-31
- Substance
- MOMETASONE FUROATE MONOHYDRATE
- Active strength
- 50 ug/1
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0781-6355-87 | 00781635587 | 1 BOTTLE, PUMP in 1 CARTON (0781-6355-87) > 120 SPRAY, METERED in 1 BOTTLE, PUMP | 2016-03-25 | 2021-10-31 | No | No | Current |