Methylphenidate Hydrochloride
- Product NDC
- 0093-5292
- 11-digit product format
- 000935292
- Labeler code
- 0093
- Product ID
- 0093-5292_cdbc33ef-8684-42b1-81bf-3e61b299f174
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methylphenidate Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Application
- ANDA078873
- Marketing category
- ANDA
- Marketing start
- 2012-09-27
- Marketing end
- 0000-00-00
- Substance
- METHYLPHENIDATE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- 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 |
|---|
| 0093-5292-01 | 00093529201 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-5292-01) | 2012-09-27 | 0000-00-00 | No | No | Current |