Methylphenidate Hydrochloride
- Product NDC
- 16714-126
- 11-digit product format
- 167140126
- Labeler code
- 16714
- Product ID
- 16714-126_0708b572-6b5d-4f9e-9183-1b694e6ac44f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methylphenidate Hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Northstar Rx LLC
- Application
- ANDA211009
- Marketing category
- ANDA
- Marketing start
- 2019-10-09
- Marketing end
- 0000-00-00
- Substance
- METHYLPHENIDATE HYDROCHLORIDE
- Active strength
- 36 mg/1
- Pharmacologic classes
- Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 16714-126-01 | 16714012601 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-126-01) | 2019-10-09 | 0000-00-00 | No | No | Current |