Nortriptyline Hydrochloride
- Product NDC
- 55700-501
- 11-digit product format
- 557000501
- Labeler code
- 55700
- Product ID
- 55700-501_5bc7116c-879f-4714-888c-8e383b127d63
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nortriptyline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Quality Care Products LLC
- Application
- ANDA075520
- Marketing category
- ANDA
- Marketing start
- 2000-05-08
- Marketing end
- 0000-00-00
- Substance
- NORTRIPTYLINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 55700-501-30 | 55700050130 | 30 CAPSULE in 1 BOTTLE (55700-501-30) | 30 capsule | 2017-02-10 | 0000-00-00 | No | No | Current |
| 55700-501-60 | 55700050160 | 60 CAPSULE in 1 BOTTLE (55700-501-60) | 60 capsule | 2017-02-10 | 0000-00-00 | No | No | Current |
| 55700-501-90 | 55700050190 | 90 CAPSULE in 1 BOTTLE (55700-501-90) | 90 capsule | 2017-02-10 | 0000-00-00 | No | No | Current |