Methylphenidate Hydrochloride
- Product NDC
- 72162-1636
- 11-digit product format
- 721621636
- Labeler code
- 72162
- Product ID
- 72162-1636_5c620170-b236-4649-9940-4f8736ee84dd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methylphenidate Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090710
- Marketing category
- ANDA
- Marketing start
- 2013-08-16
- Substance
- METHYLPHENIDATE HYDROCHLORIDE
- Active strength
- 5 mg/1
- 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/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 4B3SC438HI |
| Rxcui | 1091497 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-1636-1 | Methylphenidate Hydrochloride | 100 in 1 BOTTLE | TABLET | 100 | | 102 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-1636 | METHYLPHENIDATE HYDROCHLORIDE TABLET [BRYANT RANCH PREPACK] | 102 | Current NDC, 1 package rows | 20250403_5a22dd9b-9b48-4c96-8b20-0d20131521dc.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1636-1 | 72162163601 | 100 TABLET in 1 BOTTLE (72162-1636-1) | 100 tablet | 2013-08-16 | No | No | Historical |