Desipramine Hydrochloride
- Product NDC
- 45963-345
- 11-digit product format
- 459630345
- Labeler code
- 45963
- Product ID
- 45963-345_cb512a98-31c9-4ae9-9cc9-1d102302cfea
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Desipramine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Actavis Pharma, Inc.
- Application
- ANDA071766
- Marketing category
- ANDA
- Marketing start
- 2006-07-19
- Substance
- DESIPRAMINE HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Desipramine Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DESIPRAMINE HYDROCHLORIDE | 100 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 1Y58DO4MY1 |
| Rxcui | 1099288, 1099292, 1099296, 1099300, 1099304, 1099316 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 45963-345-02 | Desipramine Hydrochloride | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 21 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| DESIPRAMINE HYDROCHLORIDE | ACTIVE INGREDIENT | 1Y58DO4MY1 | DESIPRAMINE HYDROCHLORIDE TABLET, FILM COATED [ACTAVIS PHARMA, INC.] | 12 | |
| DESIPRAMINE | ACTIVE MOIETY | TG537D343B | DESIPRAMINE HYDROCHLORIDE TABLET, FILM COATED [ACTAVIS PHARMA, INC.] | 12 | |
| CROSCARMELLOSE SODIUM | INACTIVE INGREDIENT | M28OL1HH48 | DESIPRAMINE HYDROCHLORIDE TABLET, FILM COATED [ACTAVIS PHARMA, INC.] | 12 | |
| FD&C BLUE NO. 1 | INACTIVE INGREDIENT | H3R47K3TBD | DESIPRAMINE HYDROCHLORIDE TABLET, FILM COATED [ACTAVIS PHARMA, INC.] | 12 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | DESIPRAMINE HYDROCHLORIDE TABLET, FILM COATED [ACTAVIS PHARMA, INC.] | 12 | |
| LACTOSE MONOHYDRATE | INACTIVE INGREDIENT | EWQ57Q8I5X | DESIPRAMINE HYDROCHLORIDE TABLET, FILM COATED [ACTAVIS PHARMA, INC.] | 12 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | DESIPRAMINE HYDROCHLORIDE TABLET, FILM COATED [ACTAVIS PHARMA, INC.] | 12 | |
| POLYETHYLENE GLYCOLS | INACTIVE INGREDIENT | 3WJQ0SDW1A | DESIPRAMINE HYDROCHLORIDE TABLET, FILM COATED [ACTAVIS PHARMA, INC.] | 12 | |
| POLYSORBATE 80 | INACTIVE INGREDIENT | 6OZP39ZG8H | DESIPRAMINE HYDROCHLORIDE TABLET, FILM COATED [ACTAVIS PHARMA, INC.] | 12 | |
| POVIDONES | INACTIVE INGREDIENT | FZ989GH94E | DESIPRAMINE HYDROCHLORIDE TABLET, FILM COATED [ACTAVIS PHARMA, INC.] | 12 | |
| SODIUM LAURYL SULFATE | INACTIVE INGREDIENT | 368GB5141J | DESIPRAMINE HYDROCHLORIDE TABLET, FILM COATED [ACTAVIS PHARMA, INC.] | 12 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | DESIPRAMINE HYDROCHLORIDE TABLET, FILM COATED [ACTAVIS PHARMA, INC.] | 12 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 45963-345 | DESIPRAMINE HYDROCHLORIDE TABLET, FILM COATED [ACTAVIS PHARMA, INC.] | 19 | Current NDC, Legacy NDC, 1 package rows | 20241114_ba02a95d-d82e-4a13-90b4-a219abc0249a.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 |
|---|
| 45963-345-02 | 45963034502 | 100 TABLET, FILM COATED in 1 BOTTLE (45963-345-02) | 2006-07-19 | 0000-00-00 | No | No | Current |