Nortriptyline Hydrochloride
- Product NDC
- 43063-897
- 11-digit product format
- 430630897
- Labeler code
- 43063
- Product ID
- 43063-897_e6d91c95-5eb1-f9fb-e053-2995a90a54d5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nortriptyline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA075520
- Marketing category
- ANDA
- Marketing start
- 2000-05-08
- Marketing end
- 0000-00-00
- Substance
- NORTRIPTYLINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43063-897 | NORTRIPTYLINE HYDROCHLORIDE CAPSULE [PD-RX PHARMACEUTICALS, INC.] | 19 | Legacy NDC | 20240327_bdfac553-db8d-4bbd-b663-a03f57876867.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43063-897-30 | 43063089730 | 30 CAPSULE in 1 BOTTLE, PLASTIC (43063-897-30) | 30 capsule | 2018-09-19 | 0000-00-00 | No | No | Current |