Mometasone Furoate
- Product NDC
- 71335-2873
- 11-digit product format
- 713352873
- Labeler code
- 71335
- Product ID
- 71335-2873_0a05ffd4-01aa-4f40-9695-ea3b36154af9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mometasone Furoate
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076679
- Marketing category
- ANDA
- Marketing start
- 2004-12-21
- 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 |
|---|
| 71335-2873-1 | 71335287301 | 1 TUBE in 1 CARTON (71335-2873-1) / 15 g in 1 TUBE | 1 tube | 2025-10-24 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Mometasone Furoate | Bryant Ranch Prepack | 2025-10-24 | HUMAN PRESCRIPTION DRUG LABEL | 100 |