Amitriptyline Hydrochloride
- Product NDC
- 51079-131
- 11-digit product format
- 510790131
- Labeler code
- 51079
- Product ID
- 51079-131_b4dca9ec-6443-a7e7-e053-2a95a90ad720
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- amitriptyline hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA086009
- Marketing category
- ANDA
- Marketing start
- 1994-02-16
- Marketing end
- 2021-02-28
- Substance
- AMITRIPTYLINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 51079-131-20 | 51079013120 | 100 BLISTER PACK in 1 CARTON (51079-131-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-131-01) | 100 blister pack | 1994-02-16 | 2021-02-28 | No | No | Current |