Amitriptyline Hydrochloride
- Product NDC
- 63629-6311
- 11-digit product format
- 636296311
- Labeler code
- 63629
- Product ID
- 63629-6311_1c32a6f4-94da-448d-a3a4-78b48007fb66
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- amitriptyline hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA086009
- Marketing category
- ANDA
- Marketing start
- 1978-04-10
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-6311-1 | 63629631101 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-6311-1) | 2015-08-10 | 0000-00-00 | No | No | Current |
| 63629-6311-2 | 63629631102 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-6311-2) | 2015-08-10 | 0000-00-00 | No | No | Current |
| 63629-6311-3 | 63629631103 | 60 TABLET, FILM COATED in 1 BOTTLE (63629-6311-3) | 2015-08-10 | 0000-00-00 | No | No | Current |
| 63629-6311-4 | 63629631104 | 270 TABLET, FILM COATED in 1 BOTTLE (63629-6311-4) | 2015-08-10 | 0000-00-00 | No | No | Current |