Nortriptyline Hydrochloride
- Product NDC
- 66336-973
- 11-digit product format
- 663360973
- Labeler code
- 66336
- Product ID
- 66336-973_8194964b-a7fb-4f75-98b4-3a48f4f20a34
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nortriptyline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Dispensing Solutions, Inc.
- Application
- ANDA074132
- Marketing category
- ANDA
- Marketing start
- 1995-04-05
- Marketing end
- 0000-00-00
- Substance
- NORTRIPTYLINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 66336-973-30 | Nortriptyline Hydrochloride | 30 in 1 BOTTLE, PLASTIC | CAPSULE | 30 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 66336-973 | NORTRIPTYLINE HYDROCHLORIDE CAPSULE [DISPENSING SOLUTIONS, INC.] | 3 | Legacy NDC, 1 package rows | 20131105_f0ade32e-ac28-4d81-85a6-4eb55a39ce65.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 66336-973-30 | 66336097330 | 30 in 1 BOTTLE, PLASTIC | Historical |