Mometasone Furoate
- Product NDC
- 71205-413
- 11-digit product format
- 712050413
- Labeler code
- 71205
- Product ID
- 71205-413_c08fcb0d-7fff-4d90-aeb8-e912b930bf3d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mometasone Furoate
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Proficient Rx LP
- Application
- ANDA076067
- Marketing category
- ANDA
- Marketing start
- 2008-07-18
- 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
- 2026-12-31
- Current FDA listing
- Yes
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 | Sample | Exclude flag | Status |
|---|
| 71205-413-15 | 71205041315 | 1 TUBE in 1 CARTON (71205-413-15) / 15 g in 1 TUBE | 1 tube | 2020-02-26 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Mometasone Furoate | Proficient Rx LP | 2020-02-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |