Nortriptyline Hydrochloride
- Product NDC
- 70518-3543
- 11-digit product format
- 705183543
- Labeler code
- 70518
- Product ID
- 70518-3543_e9eb354f-e61f-6a3a-e053-2995a90ae200
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nortriptyline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA073556
- Marketing category
- ANDA
- Marketing start
- 2022-09-30
- Marketing end
- 0000-00-00
- Substance
- NORTRIPTYLINE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3543-0 | 70518354300 | 30 CAPSULE in 1 BLISTER PACK (70518-3543-0) | 30 capsule | 2022-09-30 | 0000-00-00 | No | No | Current |