METHYLPHENIDATE HYDROCHLORIDE
- Product NDC
- 50268-528
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METHYLPHENIDATE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvPAK
- Application
- ANDA207416
- Marketing category
- ANDA
- Substance
- METHYLPHENIDATE HYDROCHLORIDE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 50268-528-15 | 50 BLISTER PACK in 1 BOX (50268-528-15) / 1 TABLET in 1 BLISTER PACK (50268-528-11) | 2020-07-10 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| METHYLPHENIDATE HYDROCHLORIDE | AvPAK | 2024-01-09 | HUMAN PRESCRIPTION DRUG LABEL | 4 |