Amitriptyline Hydrochloride
- Product NDC
- 76420-698
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amitriptyline Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Asclemed USA, Inc.
- Application
- ANDA214548
- Marketing category
- ANDA
- Substance
- AMITRIPTYLINE HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 76420-698-01 | 100 TABLET, FILM COATED in 1 BOTTLE (76420-698-01) | 2024-03-02 | | No | Historical |
| 76420-698-30 | 30 TABLET, FILM COATED in 1 BOTTLE (76420-698-30) | 2024-03-02 | | No | Historical |
| 76420-698-60 | 60 TABLET, FILM COATED in 1 BOTTLE (76420-698-60) | 2024-03-02 | | No | Historical |
| 76420-698-90 | 90 TABLET, FILM COATED in 1 BOTTLE (76420-698-90) | 2024-03-02 | | No | Historical |