Amitriptyline Hydrochloride
- Product NDC
- 55154-7898
- 11-digit product format
- 551547898
- Labeler code
- 55154
- Product ID
- 55154-7898_930bd7f3-8e6f-4702-89e2-05102c2ae350
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amitriptyline Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cardinal Health 107, LLC
- Application
- ANDA085966
- Marketing category
- ANDA
- Marketing start
- 2009-06-10
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55154-7898-0 | 55154789800 | 10 BLISTER PACK in 1 BAG (55154-7898-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 10 blister pack | 2009-06-10 | 0000-00-00 | No | No | Current |