Amitriptyline HCL
- Product NDC
- 80425-0137
- 11-digit product format
- 804250137
- Labeler code
- 80425
- Product ID
- 80425-0137_ec068135-5acf-eac3-e053-2a95a90a0bd8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amitriptyline HCL
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Advanced Rx Pharmacy of Tennessee, LLC
- Application
- ANDA202446
- Marketing category
- ANDA
- Marketing start
- 2014-12-05
- 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
- 2023-12-31
- 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 |
|---|
| 80425-0137-1 | 80425013701 | 30 TABLET, FILM COATED in 1 BOTTLE (80425-0137-1) | 2014-12-05 | 0000-00-00 | No | No | Current |