Nortriptyline Hydrochloride
- Product NDC
- 51862-945
- 11-digit product format
- 518620945
- Labeler code
- 51862
- Product ID
- 51862-945_a7804223-4fad-40cf-96c1-c3ee2cbd1fd1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nortriptyline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Mayne Pharma Inc.
- Application
- ANDA073556
- Marketing category
- ANDA
- Marketing start
- 2019-12-12
- Marketing end
- 0000-00-00
- Substance
- NORTRIPTYLINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
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 |
|---|
| 51862-945-01 | 51862094501 | 100 CAPSULE in 1 BOTTLE, PLASTIC (51862-945-01) | 100 capsule | 2019-12-12 | 0000-00-00 | No | No | Current |
| 51862-945-05 | 51862094505 | 500 CAPSULE in 1 BOTTLE, PLASTIC (51862-945-05) | 500 capsule | 2019-12-12 | 0000-00-00 | No | No | Current |