Nortriptyline Hydrochloride
- Product NDC
- 45865-371
- 11-digit product format
- 458650371
- Labeler code
- 45865
- Product ID
- 45865-371_715d4c21-4a5f-cd4b-e053-2a95a90a9e21
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nortriptyline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Medsource Pharmaceuticals
- Application
- ANDA075520
- Marketing category
- ANDA
- Marketing start
- 2000-05-08
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 45865-371-30 | Nortriptyline Hydrochloride | 30 in 1 BOTTLE | CAPSULE | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 45865-371 | NORTRIPTYLINE HYDROCHLORIDE CAPSULE [MEDSOURCE PHARMACEUTICALS] | 1 | Legacy NDC, 1 package rows | 20180719_715d4c21-4a5e-cd4b-e053-2a95a90a9e21.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 45865-371-30 | 45865037130 | 30 in 1 BOTTLE | Historical |