Amitriptyline Hydrochloride
- Product NDC
- 63629-1368
- 11-digit product format
- 636291368
- Labeler code
- 63629
- Product ID
- 63629-1368_9b02f577-2a7e-1a2e-e67c-3a037eaa5200
- 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
- 50 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 |
|---|
| 63629-1368-1 | 63629136801 | 100 TABLET, FILM COATED in 1 BOTTLE (63629-1368-1) | 2004-12-28 | 0000-00-00 | No | No | Current |
| 63629-1368-2 | 63629136802 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-1368-2) | 2004-12-28 | 0000-00-00 | No | No | Current |
| 63629-1368-3 | 63629136803 | 60 TABLET, FILM COATED in 1 BOTTLE (63629-1368-3) | 2004-12-28 | 0000-00-00 | No | No | Current |
| 63629-1368-4 | 63629136804 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-1368-4) | 2004-12-28 | 0000-00-00 | No | No | Current |
| 63629-1368-5 | 63629136805 | 20 TABLET, FILM COATED in 1 BOTTLE (63629-1368-5) | 2004-12-28 | 0000-00-00 | No | No | Current |
| 63629-1368-6 | 63629136806 | 28 TABLET, FILM COATED in 1 BOTTLE (63629-1368-6) | 2004-12-28 | 0000-00-00 | No | No | Current |
| 63629-1368-7 | 63629136807 | 56 TABLET, FILM COATED in 1 BOTTLE (63629-1368-7) | 2004-12-28 | 0000-00-00 | No | No | Current |
| 63629-1368-8 | 63629136808 | 180 TABLET, FILM COATED in 1 BOTTLE (63629-1368-8) | 2005-03-08 | 0000-00-00 | No | No | Current |