Amitriptyline hydrochloride
- Product NDC
- 0832-1221
- 11-digit product format
- 008321221
- Labeler code
- 0832
- Product ID
- 0832-1221_815dded0-4513-4620-ac79-ef7b8f9becb2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amitriptyline hydrochloride
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Upsher-Smith Laboratories, LLC
- Application
- ANDA212654
- Marketing category
- ANDA
- Marketing start
- 2020-04-07
- Marketing end
- 0000-00-00
- Substance
- AMITRIPTYLINE HYDROCHLORIDE
- Active strength
- 25 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 |
|---|
| 0832-1221-10 | 00832122110 | 1000 TABLET, COATED in 1 BOTTLE (0832-1221-10) | 2021-09-29 | 0000-00-00 | No | No | Current |
| 0832-1221-11 | 00832122111 | 100 TABLET, COATED in 1 BOTTLE (0832-1221-11) | 2021-09-29 | 0000-00-00 | No | No | Current |