Amitriptyline hydrochloride
- Product NDC
- 0832-1225
- 11-digit product format
- 008321225
- Labeler code
- 0832
- Product ID
- 0832-1225_df2f4608-bd27-4bc8-bb44-6d934435efc8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amitriptyline hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Upsher-smith Laboratories, LLC
- Application
- ANDA212654
- Marketing category
- ANDA
- Marketing start
- 2021-09-29
- Marketing end
- 0000-00-00
- Substance
- AMITRIPTYLINE HYDROCHLORIDE
- Active strength
- 150 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 |
|---|
| 0832-1225-11 | 00832122511 | 100 TABLET, FILM COATED in 1 BOTTLE (0832-1225-11) | 2021-09-29 | 0000-00-00 | No | No | Current |