Amitriptyline Hydrochloride
- Product NDC
- 63629-2117
- 11-digit product format
- 636292117
- Labeler code
- 63629
- Product ID
- 63629-2117_cfd13c0c-d944-4d7c-b7d8-bb57e97811d4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amitriptyline Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA040218
- Marketing category
- ANDA
- Marketing start
- 1997-09-11
- 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
- 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 |
|---|
| 63629-2117-1 | 63629211701 | 100 TABLET, FILM COATED in 1 BOTTLE (63629-2117-1) | 2021-02-01 | 0000-00-00 | No | No | Current |