AMITRIPTYLINE HYDROCHLORIDE
- Product NDC
- 61919-013
- 11-digit product format
- 619190013
- Labeler code
- 61919
- Product ID
- 61919-013_9c59436c-7b89-3cf8-e053-2a95a90a2863
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AMITRIPTYLINE HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Direct Rx
- Application
- ANDA086009
- Marketing category
- ANDA
- Marketing start
- 2014-01-01
- Marketing end
- 0000-00-00
- Substance
- AMITRIPTYLINE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-013-30 | 61919001330 | 30 TABLET, FILM COATED in 1 BOTTLE (61919-013-30) | 2014-04-01 | 0000-00-00 | No | No | Current |
| 61919-013-71 | 61919001371 | 100 TABLET, FILM COATED in 1 BOTTLE (61919-013-71) | 2016-03-04 | 0000-00-00 | No | No | Current |
| 61919-013-90 | 61919001390 | 90 TABLET, FILM COATED in 1 BOTTLE (61919-013-90) | 2016-03-04 | 0000-00-00 | No | No | Current |