Amitriptyline Hydrochloride
- Product NDC
- 67296-1245
- 11-digit product format
- 672961245
- Labeler code
- 67296
- Product ID
- 67296-1245_9c9ef37e-ad18-8a77-e053-2995a90adfe6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amitriptyline Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA086009
- Marketing category
- ANDA
- Marketing start
- 1978-04-10
- 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
- 2021-12-31
- 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 |
|---|
| 67296-1245-1 | 67296124501 | 15 TABLET, FILM COATED in 1 BOTTLE (67296-1245-1) | 1978-04-10 | 0000-00-00 | No | No | Current |