Mometasone Furoate
- Product NDC
- 0168-0270
- 11-digit product format
- 001680270
- Labeler code
- 0168
- Product ID
- 0168-0270_e5e151c4-74f1-470a-a1cb-bde40891a5ee
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- mometasone furoate
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.
- Application
- ANDA076171
- Marketing category
- ANDA
- Marketing start
- 2005-04-08
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0168-0270-15 | 00168027015 | 15 g in 1 TUBE (0168-0270-15) | 15 g | 2005-04-08 | 0000-00-00 | No | No | Current |
| 0168-0270-46 | 00168027046 | 45 g in 1 TUBE (0168-0270-46) | 45 g | 2005-04-08 | 0000-00-00 | No | No | Current |