Ramelteon
- Product NDC
- 51407-375
- 11-digit product format
- 514070375
- Labeler code
- 51407
- Product ID
- 51407-375_dc67e0ca-7a69-1f2f-e053-2995a90af42a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ramelteon
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA091693
- Marketing category
- ANDA
- Marketing start
- 2013-07-26
- Marketing end
- 0000-00-00
- Substance
- RAMELTEON
- Active strength
- 8 mg/1
- Pharmacologic classes
- Melatonin Receptor Agonist [EPC], Melatonin Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 51407-375-30 | 51407037530 | 30 TABLET in 1 BOTTLE (51407-375-30) | 30 tablet | 2020-03-25 | 0000-00-00 | No | No | Current |