Mometasone Furoate
- Product NDC
- 16714-974
- 11-digit product format
- 167140974
- Labeler code
- 16714
- Product ID
- 16714-974_9e26d245-e65d-4360-90cb-41ee39aea6d9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mometasone Furoate
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- NORTHSTAR RX LLC
- Application
- ANDA078541
- Marketing category
- ANDA
- Marketing start
- 2019-09-17
- Marketing end
- 0000-00-00
- Substance
- MOMETASONE FUROATE
- Active strength
- 1 mg/g
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 16714-974-01 | 16714097401 | 15 g in 1 TUBE (16714-974-01) | 15 g | 2019-09-17 | 0000-00-00 | No | No | Current |
| 16714-974-02 | 16714097402 | 45 g in 1 TUBE (16714-974-02) | 45 g | 2019-09-17 | 0000-00-00 | No | No | Current |