Nortriptyline Hydrochloride
- Product NDC
- 71335-2199
- 11-digit product format
- 713352199
- Labeler code
- 71335
- Product ID
- 71335-2199_5df187ff-c2fc-4b14-b727-ec8391ff295f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nortriptyline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA073556
- Marketing category
- ANDA
- Marketing start
- 2019-12-12
- Marketing end
- 0000-00-00
- Substance
- NORTRIPTYLINE HYDROCHLORIDE
- Active strength
- 75 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 |
|---|
| 71335-2199-1 | 71335219901 | 30 CAPSULE in 1 BOTTLE, PLASTIC (71335-2199-1) | 30 capsule | 2022-12-12 | 0000-00-00 | No | No | Current |
| 71335-2199-2 | 71335219902 | 60 CAPSULE in 1 BOTTLE, PLASTIC (71335-2199-2) | 60 capsule | 2022-12-12 | 0000-00-00 | No | No | Current |
| 71335-2199-3 | 71335219903 | 90 CAPSULE in 1 BOTTLE, PLASTIC (71335-2199-3) | 90 capsule | 2022-12-12 | 0000-00-00 | No | No | Current |
| 71335-2199-4 | 71335219904 | 28 CAPSULE in 1 BOTTLE, PLASTIC (71335-2199-4) | 28 capsule | 2022-12-12 | 0000-00-00 | No | No | Current |