Amitriptyline Hydrochloride
- Product NDC
- 60760-907
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amitriptyline Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- ST. MARY'S MEDICAL PARK PHARMACY
- Application
- ANDA214548
- Marketing category
- ANDA
- Substance
- AMITRIPTYLINE HYDROCHLORIDE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 60760-907-90 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-907-90) | 2024-06-12 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Amitriptyline Hydrochloride Tablets, USP Rx Only | ST. MARY'S MEDICAL PARK PHARMACY | 2024-06-18 | HUMAN PRESCRIPTION DRUG LABEL | 1 |