Nortriptyline Hydrochloride
- Product NDC
- 71335-1773
- 11-digit product format
- 713351773
- Labeler code
- 71335
- Product ID
- 71335-1773_529c7d27-1a3f-4a94-a558-522bf102f37f
- 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
- 50 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 |
|---|
| 71335-1773-1 | 71335177301 | 30 CAPSULE in 1 BOTTLE, PLASTIC (71335-1773-1) | 30 capsule | 2021-03-11 | 0000-00-00 | No | No | Current |
| 71335-1773-2 | 71335177302 | 60 CAPSULE in 1 BOTTLE, PLASTIC (71335-1773-2) | 60 capsule | 2021-03-11 | 0000-00-00 | No | No | Current |
| 71335-1773-3 | 71335177303 | 90 CAPSULE in 1 BOTTLE, PLASTIC (71335-1773-3) | 90 capsule | 2021-03-11 | 0000-00-00 | No | No | Current |
| 71335-1773-4 | 71335177304 | 28 CAPSULE in 1 BOTTLE, PLASTIC (71335-1773-4) | 28 capsule | 2021-03-11 | 0000-00-00 | No | No | Current |
| 71335-1773-5 | 71335177305 | 120 CAPSULE in 1 BOTTLE, PLASTIC (71335-1773-5) | 120 capsule | 2021-03-11 | 0000-00-00 | No | No | Current |