Methylphenidate hydrochloride
- Product NDC
- 47781-416
- 11-digit product format
- 477810416
- Labeler code
- 47781
- Product ID
- 47781-416_b32ff40d-bd27-9c66-4627-63e7832934aa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methylphenidate hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Alvogen Inc.
- Application
- ANDA210818
- Marketing category
- ANDA
- Marketing start
- 2018-11-30
- Marketing end
- 2022-11-01
- Substance
- METHYLPHENIDATE HYDROCHLORIDE
- Active strength
- 27 mg/1
- Pharmacologic classes
- Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE]
- DEA schedule
- CII
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 47781-416-01 | 47781041601 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47781-416-01) | 2019-01-09 | 2022-11-01 | No | No | Current |