Mometasone Furoate
- Product NDC
- 70518-3244
- 11-digit product format
- 705183244
- Labeler code
- 70518
- Product ID
- 70518-3244_e39b1714-5c4c-7c6f-e053-2a95a90a4cfc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mometasone Furoate
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA076067
- Marketing category
- ANDA
- Marketing start
- 2021-10-15
- Marketing end
- 0000-00-00
- Substance
- MOMETASONE FUROATE
- Active strength
- 1 mg/g
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 04201GDN4R | MOMETASONE FUROATE | 83919-23-7 | MOMETASONE FUROATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3244-0 | 70518324400 | 1 TUBE in 1 CARTON (70518-3244-0) > 15 g in 1 TUBE | 1 tube | 2021-10-15 | 0000-00-00 | No | No | Current |