Mometasone Furoate
- Product NDC
- 0713-0701
- 11-digit product format
- 007130701
- Labeler code
- 0713
- Product ID
- 0713-0701_e22c7d66-d4d7-8812-e053-2a95a90ac681
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mometasone Furoate
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Cosette Pharmaceuticals, Inc.
- Application
- ANDA077678
- Marketing category
- ANDA
- Marketing start
- 2014-03-04
- Marketing end
- 2023-09-30
- Substance
- MOMETASONE FUROATE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0713-0701-53 | 00713070153 | 1 BOTTLE in 1 CARTON (0713-0701-53) > 60 mL in 1 BOTTLE | 1 bottle | 2014-03-04 | 0000-00-00 | No | No | Current |
| 0713-0701-85 | 00713070185 | 1 BOTTLE in 1 CARTON (0713-0701-85) > 30 mL in 1 BOTTLE | 1 bottle | 2014-03-04 | 0000-00-00 | No | No | Current |