AMITRIPTYLINE HYDROCHLORIDE
- Product NDC
- 55700-600
- 11-digit product format
- 557000600
- Labeler code
- 55700
- Product ID
- 55700-600_0f12f50f-7087-46e7-a2e6-356b4c566c9f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AMITRIPTYLINE HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Quality Care Products LLC
- Application
- ANDA202446
- Marketing category
- ANDA
- Marketing start
- 2018-04-13
- 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 |
|---|
| 55700-600-00 | 55700060000 | 100 TABLET, FILM COATED in 1 BOTTLE (55700-600-00) | 2018-04-13 | 0000-00-00 | No | No | Current |
| 55700-600-30 | 55700060030 | 30 TABLET, FILM COATED in 1 BOTTLE (55700-600-30) | 2018-05-04 | 0000-00-00 | No | No | Current |
| 55700-600-60 | 55700060060 | 60 TABLET, FILM COATED in 1 BOTTLE (55700-600-60) | 2018-05-04 | 0000-00-00 | No | No | Current |
| 55700-600-90 | 55700060090 | 90 TABLET, FILM COATED in 1 BOTTLE (55700-600-90) | 2018-05-04 | 0000-00-00 | No | No | Current |