Risperidone
- Product NDC
- 59746-030
- 11-digit product format
- 597460030
- Labeler code
- 59746
- Product ID
- 59746-030_90b80768-87f7-4fb1-8142-909dba9555e2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Risperidone
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- Jubilant Cadista Pharmacuticals Inc.
- Application
- ANDA090839
- Marketing category
- ANDA
- Marketing start
- 2011-11-04
- Substance
- RISPERIDONE
- Active strength
- 2 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Risperidone
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| RISPERIDONE | 2 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L6UH7ZF8HC |
| Rxcui | 401953, 401954, 403825, 616698, 616705 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 59746-030-22 | Risperidone | 7 in 1 CARTON | TABLET, ORALLY DISINTEGRATING | 7 | | 25 |
| 59746-030-22 | Risperidone | 4 in 1 BLISTER PACK | TABLET, ORALLY DISINTEGRATING | 4 | | 25 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| Risperidone | ACTIVE INGREDIENT | L6UH7ZF8HC | RISPERIDONE (RISPERIDONE) TABLET, ORALLY DISINTEGRATING [JUBILANT CADISTA PHARMACEUTICALS INC.] | 11 | |
| Risperidone | ACTIVE MOIETY | L6UH7ZF8HC | RISPERIDONE (RISPERIDONE) TABLET, ORALLY DISINTEGRATING [JUBILANT CADISTA PHARMACEUTICALS INC.] | 11 | |
| Acesulfame Potassium | INACTIVE INGREDIENT | 23OV73Q5G9 | RISPERIDONE (RISPERIDONE) TABLET, ORALLY DISINTEGRATING [JUBILANT CADISTA PHARMACEUTICALS INC.] | 11 | |
| Aspartame | INACTIVE INGREDIENT | Z0H242BBR1 | RISPERIDONE (RISPERIDONE) TABLET, ORALLY DISINTEGRATING [JUBILANT CADISTA PHARMACEUTICALS INC.] | 11 | |
| Dimethylaminoethyl Methacrylate - Butyl Methacrylate - Methyl Methacrylate Copolymer | INACTIVE INGREDIENT | 905HNO1SIH | RISPERIDONE (RISPERIDONE) TABLET, ORALLY DISINTEGRATING [JUBILANT CADISTA PHARMACEUTICALS INC.] | 11 | |
| Fd&c Blue No. 1 | INACTIVE INGREDIENT | H3R47K3TBD | RISPERIDONE (RISPERIDONE) TABLET, ORALLY DISINTEGRATING [JUBILANT CADISTA PHARMACEUTICALS INC.] | 11 | |
| Fd&c Yellow No. 6 | INACTIVE INGREDIENT | H77VEI93A8 | RISPERIDONE (RISPERIDONE) TABLET, ORALLY DISINTEGRATING [JUBILANT CADISTA PHARMACEUTICALS INC.] | 11 | |
| Ferric Oxide Red | INACTIVE INGREDIENT | 1K09F3G675 | RISPERIDONE (RISPERIDONE) TABLET, ORALLY DISINTEGRATING [JUBILANT CADISTA PHARMACEUTICALS INC.] | 11 | |
| Ferric Oxide Yellow | INACTIVE INGREDIENT | EX438O2MRT | RISPERIDONE (RISPERIDONE) TABLET, ORALLY DISINTEGRATING [JUBILANT CADISTA PHARMACEUTICALS INC.] | 11 | |
| Hydroxypropyl Cellulose, Low Substituted | INACTIVE INGREDIENT | 2165RE0K14 | RISPERIDONE (RISPERIDONE) TABLET, ORALLY DISINTEGRATING [JUBILANT CADISTA PHARMACEUTICALS INC.] | 11 | |
| Magnesium Aluminometasilicate Type I-a | INACTIVE INGREDIENT | 7LVU907546 | RISPERIDONE (RISPERIDONE) TABLET, ORALLY DISINTEGRATING [JUBILANT CADISTA PHARMACEUTICALS INC.] | 11 | |
| Mannitol | INACTIVE INGREDIENT | 3OWL53L36A | RISPERIDONE (RISPERIDONE) TABLET, ORALLY DISINTEGRATING [JUBILANT CADISTA PHARMACEUTICALS INC.] | 11 | |
| Peppermint | INACTIVE INGREDIENT | V95R5KMY2B | RISPERIDONE (RISPERIDONE) TABLET, ORALLY DISINTEGRATING [JUBILANT CADISTA PHARMACEUTICALS INC.] | 11 | |
| Silicon Dioxide | INACTIVE INGREDIENT | ETJ7Z6XBU4 | RISPERIDONE (RISPERIDONE) TABLET, ORALLY DISINTEGRATING [JUBILANT CADISTA PHARMACEUTICALS INC.] | 11 | |
| Sodium Chloride | INACTIVE INGREDIENT | 451W47IQ8X | RISPERIDONE (RISPERIDONE) TABLET, ORALLY DISINTEGRATING [JUBILANT CADISTA PHARMACEUTICALS INC.] | 11 | |
| Sodium Lauryl Sulfate | INACTIVE INGREDIENT | 368GB5141J | RISPERIDONE (RISPERIDONE) TABLET, ORALLY DISINTEGRATING [JUBILANT CADISTA PHARMACEUTICALS INC.] | 11 | |
| Sodium Stearyl Fumarate | INACTIVE INGREDIENT | 7CV7WJK4UI | RISPERIDONE (RISPERIDONE) TABLET, ORALLY DISINTEGRATING [JUBILANT CADISTA PHARMACEUTICALS INC.] | 11 | |
| Talc | INACTIVE INGREDIENT | 7SEV7J4R1U | RISPERIDONE (RISPERIDONE) TABLET, ORALLY DISINTEGRATING [JUBILANT CADISTA PHARMACEUTICALS INC.] | 11 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59746-030 | RISPERIDONE TABLET, ORALLY DISINTEGRATING [JUBILANT CADISTA PHARMACUTICALS INC.] | 24 | Current NDC, Legacy NDC, 2 package rows | 20250519_739dcf8a-ed73-5eb0-899b-7e51cb73c335.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 |
|---|
| 59746-030-22 | 59746003022 | 7 BLISTER PACK in 1 CARTON (59746-030-22) / 4 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK | 7 blister pack | 2011-11-04 | 0000-00-00 | No | No | Current |