Amoxapine
- Product NDC
- 62135-701
- 11-digit product format
- 621350701
- Labeler code
- 62135
- Product ID
- 62135-701_298fbb0d-737b-b42f-e063-6394a90ac69b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxapine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Chartwell RX, LLC
- Application
- ANDA072879
- Marketing category
- ANDA
- Marketing start
- 1991-06-28
- Substance
- AMOXAPINE
- Active strength
- 50 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
- Amoxapine
- Listing expiration
- 2026-12-31
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 |
|---|
| 62135-701-90 | Amoxapine | 90 in 1 BOTTLE | TABLET | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62135-701 | AMOXAPINE TABLET [CHARTWELL RX, LLC] | 2 | Current NDC, 1 package rows | 20241228_eed5e856-dd7b-4eaa-9dad-508f2bef9328.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 |
|---|
| 62135-701-90 | 62135070190 | 90 TABLET in 1 BOTTLE (62135-701-90) | 90 tablet | 2023-09-06 | No | No | Historical |