AMITRIPTYLINE HYDROCHLORIDE
- Product NDC
- 60760-367
- 11-digit product format
- 607600367
- Labeler code
- 60760
- Product ID
- 60760-367_f06e8d19-c6eb-6cba-e053-2995a90a3adb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AMITRIPTYLINE HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA202446
- Marketing category
- ANDA
- Marketing start
- 2016-06-03
- Marketing end
- 0000-00-00
- Substance
- AMITRIPTYLINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60760-367 | AMITRIPTYLINE HYDROCHLORIDE TABLET, FILM COATED [ST. MARY'S MEDICAL PARK PHARMACY] | 8 | Legacy NDC | 20231228_60a542d8-92da-0324-e053-2a91aa0a95da.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-367-00 | 60760036700 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-367-00) | 2019-10-15 | 0000-00-00 | No | No | Current |
| 60760-367-30 | 60760036730 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-367-30) | 2016-06-03 | 0000-00-00 | No | No | Current |