Amoxapine
- Product NDC
- 0591-5714
- 11-digit product format
- 005915714
- Labeler code
- 0591
- Product ID
- 0591-5714_40931661-1155-4850-baaa-227f066ed616
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxapine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Actavis Pharma, Inc.
- Application
- ANDA072691
- Marketing category
- ANDA
- Marketing start
- 1992-08-28
- Substance
- AMOXAPINE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Amoxapine
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AMOXAPINE | 50 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | R63VQ857OT |
| Rxcui | 197363, 197364, 197365, 197366 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0591-5714-01 | Amoxapine | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 20 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| AMOXAPINE | ACTIVE INGREDIENT | R63VQ857OT | AMOXAPINE TABLET [ACTAVIS PHARMA, INC.] | 12 | |
| AMOXAPINE | ACTIVE MOIETY | R63VQ857OT | AMOXAPINE TABLET [ACTAVIS PHARMA, INC.] | 12 | |
| CALCIUM PHOSPHATE, DIBASIC, DIHYDRATE | INACTIVE INGREDIENT | O7TSZ97GEP | AMOXAPINE TABLET [ACTAVIS PHARMA, INC.] | 12 | |
| FD&C BLUE NO. 2 | INACTIVE INGREDIENT | L06K8R7DQK | AMOXAPINE TABLET [ACTAVIS PHARMA, INC.] | 12 | |
| FD&C YELLOW NO. 6 | INACTIVE INGREDIENT | H77VEI93A8 | AMOXAPINE TABLET [ACTAVIS PHARMA, INC.] | 12 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | AMOXAPINE TABLET [ACTAVIS PHARMA, INC.] | 12 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | AMOXAPINE TABLET [ACTAVIS PHARMA, INC.] | 12 | |
| STEARIC ACID | INACTIVE INGREDIENT | 4ELV7Z65AP | AMOXAPINE TABLET [ACTAVIS PHARMA, INC.] | 12 | |
| AMOXAPINE | ACTIVE INGREDIENT | R63VQ857OT | AMOXAPINE TABLET [PHYSICIANS TOTAL CARE, INC.] | 1 | |
| AMOXAPINE | ACTIVE MOIETY | R63VQ857OT | AMOXAPINE TABLET [PHYSICIANS TOTAL CARE, INC.] | 1 | |
| DIBASIC CALCIUM PHOSPHATE DIHYDRATE | INACTIVE INGREDIENT | O7TSZ97GEP | AMOXAPINE TABLET [PHYSICIANS TOTAL CARE, INC.] | 1 | |
| FD&C YELLOW NO. 6 | INACTIVE INGREDIENT | H77VEI93A8 | AMOXAPINE TABLET [PHYSICIANS TOTAL CARE, INC.] | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | AMOXAPINE TABLET [PHYSICIANS TOTAL CARE, INC.] | 1 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | AMOXAPINE TABLET [PHYSICIANS TOTAL CARE, INC.] | 1 | |
| STEARIC ACID | INACTIVE INGREDIENT | 4ELV7Z65AP | AMOXAPINE TABLET [PHYSICIANS TOTAL CARE, INC.] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0591-5714 | AMOXAPINE TABLET [ACTAVIS PHARMA, INC.] | 19 | Current NDC, Legacy NDC, 1 package rows | 20241213_a16297df-3158-48db-85e5-5cd506885556.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 |
|---|
| 0591-5714-01 | 00591571401 | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5714-01) | 100 tablet | 1992-08-28 | 0000-00-00 | No | No | Current |