AMITRIPTYLINE HYDROCHLORIDE
- Product NDC
- 55700-660
- 11-digit product format
- 557000660
- Labeler code
- 55700
- Product ID
- 55700-660_8e52309b-4212-4150-8a2f-e46e93129e9a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AMITRIPTYLINE HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA202446
- Marketing category
- ANDA
- Marketing start
- 2018-07-26
- Marketing end
- 0000-00-00
- Substance
- AMITRIPTYLINE HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 55700-660-30 | 55700066030 | 30 TABLET, FILM COATED in 1 BOTTLE (55700-660-30) | 2018-07-26 | 0000-00-00 | No | No | Current |