Nortriptyline Hydrochloride
- Product NDC
- 68151-2898
- 11-digit product format
- 681512898
- Labeler code
- 68151
- Product ID
- 68151-2898_0c926b35-0fc4-4e5a-a454-d887955b05ef
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nortriptyline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- ANDA074132
- Marketing category
- ANDA
- Marketing start
- 1995-04-06
- Marketing end
- 0000-00-00
- Substance
- NORTRIPTYLINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 68151-2898-8 | Nortriptyline Hydrochloride | 1 in 1 BOTTLE | CAPSULE | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-2898 | NORTRIPTYLINE HYDROCHLORIDE CAPSULE [CARILION MATERIALS MANAGEMENT] | 3 | Legacy NDC, 1 package rows | 20160806_d7d6bdda-c1fa-44b9-8585-f80bf0830972.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68151-2898-8 | 68151289808 | 1 in 1 BOTTLE | Historical |