Mometasone Furoate
- Product NDC
- 70518-2883
- 11-digit product format
- 705182883
- Labeler code
- 70518
- Product ID
- 70518-2883_e39b5293-eb73-f990-e053-2a95a90aaef9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mometasone Furoate
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA076679
- Marketing category
- ANDA
- Marketing start
- 2020-09-14
- 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
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 |
|---|
| 70518-2883-0 | 70518288300 | 1 TUBE in 1 CARTON (70518-2883-0) > 15 g in 1 TUBE | 1 tube | 2020-09-14 | 0000-00-00 | No | No | Current |