AMITRIPTYLINE HYDROCHLORIDE
- Product NDC
- 60760-181
- 11-digit product format
- 607600181
- Labeler code
- 60760
- Product ID
- 60760-181_f06e4d37-5f31-d60c-e053-2995a90a4634
- 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
- 2018-04-27
- Marketing end
- 0000-00-00
- Substance
- AMITRIPTYLINE HYDROCHLORIDE
- Active strength
- 75 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 |
|---|
| 60760-181-30 | 60760018130 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-181-30) | 2018-04-27 | 0000-00-00 | No | No | Current |