AMITRIPTYLINE HYDROCHLORIDE
- Product NDC
- 50090-3026
- 11-digit product format
- 500903026
- Labeler code
- 50090
- Product ID
- 50090-3026_4b0b0df1-2da7-404d-9dc2-1ea58417452f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AMITRIPTYLINE HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA202446
- Marketing category
- ANDA
- Marketing start
- 2014-12-05
- Marketing end
- 0000-00-00
- Substance
- AMITRIPTYLINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3026 | AMITRIPTYLINE HYDROCHLORIDE TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 9 | Legacy NDC | 20240202_d8926880-b4cd-4b22-ae01-005a4c52bdee.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-3026-0 | 50090302600 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-3026-0) | 2018-02-22 | 0000-00-00 | No | No | Current |
| 50090-3026-1 | 50090302601 | 100 TABLET, FILM COATED in 1 BOTTLE (50090-3026-1) | 2017-05-26 | 0000-00-00 | No | No | Current |
| 50090-3026-6 | 50090302606 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-3026-6) | 2017-05-30 | 0000-00-00 | No | No | Current |