Methylphenidate
- Product NDC
- 0781-2362
- 11-digit product format
- 007812362
- Labeler code
- 0781
- Product ID
- 0781-2362_2a42277a-d670-4bae-b49d-fd1d8e13afff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methylphenidate
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Sandoz Inc
- Application
- NDA021284
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2015-11-24
- Marketing end
- 2027-04-30
- Substance
- METHYLPHENIDATE HYDROCHLORIDE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE]
- DEA schedule
- CII
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Methylphenidate
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| METHYLPHENIDATE HYDROCHLORIDE | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 4B3SC438HI |
| Rxcui | 1806177, 1806179, 1806183, 1806195 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0781-2362-01 | Methylphenidate | 100 in 1 BOTTLE | CAPSULE, EXTENDED RELEASE | 100 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0781-2362 | METHYLPHENIDATE CAPSULE, EXTENDED RELEASE [SANDOZ INC] | 7 | Current NDC, Legacy NDC, 1 package rows | 20240302_1f8983ce-71b8-4c62-830d-e4692ddededa.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0781-2362-01 | 00781236201 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0781-2362-01) | 2015-11-24 | 2026-11-30 | No | No | Current |