Thioridazine Hydrochloride
- Product NDC
- 62135-938
- 11-digit product format
- 621350938
- Labeler code
- 62135
- Product ID
- 62135-938_2e81bd7d-c434-2d02-e063-6294a90a196d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Thioridazine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Chartwell RX, LLC
- Application
- ANDA088134
- Marketing category
- ANDA
- Marketing start
- 1983-08-30
- Substance
- THIORIDAZINE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Phenothiazine [EPC], Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Thioridazine Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| THIORIDAZINE HYDROCHLORIDE | 50 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 4WCI67NK8M |
| Rxcui | 198270, 198274, 198275, 313354 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 62135-938-90 | Thioridazine Hydrochloride | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62135-938 | THIORIDAZINE HYDROCHLORIDE TABLET, FILM COATED [CHARTWELL RX, LLC] | 1 | Current NDC, 1 package rows | 20250223_e0bbe982-6434-468b-bd29-64ac57386fbe.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 62135-938-90 | 62135093890 | 90 TABLET, FILM COATED in 1 BOTTLE (62135-938-90) | 2025-02-14 | No | No | Historical |