Nortriptyline Hydrochloride
- Product NDC
- 51862-015
- 11-digit product format
- 518620015
- Labeler code
- 51862
- Product ID
- 51862-015_912a2e7c-3615-4dff-b8b8-27eed882ab3f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nortriptyline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Mayne Pharma Inc.
- Application
- ANDA073556
- Marketing category
- ANDA
- Marketing start
- 2016-06-01
- Marketing end
- 2021-05-31
- Substance
- NORTRIPTYLINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51862-015-01 | Nortriptyline Hydrochloride | 100 in 1 BOTTLE, PLASTIC | CAPSULE | 100 | | 9 |
| 51862-015-05 | Nortriptyline Hydrochloride | 500 in 1 BOTTLE, PLASTIC | CAPSULE | 500 | | 9 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51862-015 | NORTRIPTYLINE HYDROCHLORIDE CAPSULE [MAYNE PHARMA INC.] | 9 | Legacy NDC, 2 package rows | 20210325_765d726b-fd4b-4ef7-afd7-9e7e9bf8cae6.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 |
|---|
| 51862-015-01 | 51862001501 | 100 CAPSULE in 1 BOTTLE, PLASTIC (51862-015-01) | 100 capsule | 2016-06-01 | 2021-05-31 | No | No | Current |
| 51862-015-05 | 51862001505 | 500 CAPSULE in 1 BOTTLE, PLASTIC (51862-015-05) | 500 capsule | 2016-06-01 | 2021-05-31 | No | No | Current |