Modafinil
- Product NDC
- 55700-695
- 11-digit product format
- 557000695
- Labeler code
- 55700
- Product ID
- 55700-695_e4dd5920-575d-437a-af59-b18c20a154f8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- modafinil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA077667
- Marketing category
- ANDA
- Marketing start
- 2018-11-02
- Marketing end
- 0000-00-00
- Substance
- MODAFINIL
- Active strength
- 200 mg/1
- Pharmacologic classes
- Central Nervous System Stimulation [PE],Increased Sympathetic Activity [PE],Sympathomimetic-like Agent [EPC]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 55700-695-30 | 55700069530 | 30 TABLET in 1 BOTTLE (55700-695-30) | 30 tablet | 2018-11-02 | 0000-00-00 | No | No | Current |