Methylphenidate Hydrochloride
- Product NDC
- 43598-438
- 11-digit product format
- 435980438
- Labeler code
- 43598
- Product ID
- 43598-438_b2e44e65-bff9-7e54-c9e9-6adf1b831b6f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methylphenidate Hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Dr.Reddys Laboratories Inc
- Application
- ANDA213473
- Marketing category
- ANDA
- Marketing start
- 2020-08-20
- Marketing end
- 0000-00-00
- Substance
- METHYLPHENIDATE HYDROCHLORIDE
- Active strength
- 18 mg/1
- Pharmacologic classes
- Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 43598-438-01 | Methylphenidate Hydrochloride | 100 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 100 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43598-438 | METHYLPHENIDATE HYDROCHLORIDE TABLET, EXTENDED RELEASE [DR.REDDYS LABORATORIES INC] | 5 | Legacy NDC, 1 package rows | 20200820_7124df7e-6273-a68d-6e35-dc06122d8686.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 |
|---|
| 43598-438-01 | 43598043801 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (43598-438-01) | 2020-08-20 | 0000-00-00 | No | No | Current |