Methylphenidate Hydrochloride
- Product NDC
- 67877-602
- 11-digit product format
- 678770602
- Labeler code
- 67877
- Product ID
- 67877-602_2a496565-0f45-49a8-b49b-e4a734aee439
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methylphenidate Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Ascend Laboratories, LLC
- Application
- ANDA211647
- Marketing category
- ANDA
- Marketing start
- 2020-04-01
- Substance
- METHYLPHENIDATE HYDROCHLORIDE
- Active strength
- 5 mg/5mL
- Pharmacologic classes
- Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Methylphenidate Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| METHYLPHENIDATE HYDROCHLORIDE | 5 mg/5mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 4B3SC438HI |
| Rxcui | 1091133, 1091341 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67877-602-91 | Methylphenidate Hydrochloride | 500 mL in 1 BOTTLE | SOLUTION | 500 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67877-602 | METHYLPHENIDATE HYDROCHLORIDE SOLUTION [ASCEND LABORATORIES, LLC] | 5 | Current NDC, Legacy NDC, 1 package rows | 20211230_5fa3da25-13aa-4ee3-acf5-cd505f4688d0.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67877-602-91 | 67877060291 | 500 mL in 1 BOTTLE (67877-602-91) | 500 ml | 2020-04-01 | 0000-00-00 | No | No | Current |