Nortriptyline Hydrochloride
- Product NDC
- 60760-811
- 11-digit product format
- 607600811
- Labeler code
- 60760
- Product ID
- 60760-811_7aca25ab-0948-371b-e053-2a91aa0a0fc0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nortriptyline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA075520
- Marketing category
- ANDA
- Marketing start
- 2017-03-16
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60760-811 | NORTRIPTYLINE HYDROCHLORIDE CAPSULE [ST. MARY'S MEDICAL PARK PHARMACY] | 3 | Legacy NDC | 20181117_60c9f9d7-2906-33f7-e053-2a91aa0a9713.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-811-30 | 60760081130 | 30 CAPSULE in 1 BOTTLE, PLASTIC (60760-811-30) | 30 capsule | 2017-03-16 | 0000-00-00 | No | No | Current |