AMITRIPTYLINE HYDROCHLORIDE
- Product NDC
- 69306-050
- 11-digit product format
- 693060050
- Labeler code
- 69306
- Product ID
- 69306-050_c479d482-243c-2bb3-e053-2a95a90a0b0b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AMITRIPTYLINE HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Doc Rx
- Application
- ANDA202446
- Marketing category
- ANDA
- Marketing start
- 2014-12-05
- Marketing end
- 0000-00-00
- Substance
- AMITRIPTYLINE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69306-050 | AMITRIPTYLINE HYDROCHLORIDE TABLET, FILM COATED [DOC RX] | 2 | Legacy NDC | 20210613_dc8d3a55-043d-41d9-bb7a-d33d965b095d.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69306-050-03 | 69306005003 | 30 TABLET, FILM COATED in 1 BOTTLE (69306-050-03) | 2020-02-12 | 0000-00-00 | No | No | Current |
| 69306-050-06 | 69306005006 | 60 TABLET, FILM COATED in 1 BOTTLE (69306-050-06) | 2020-02-12 | 0000-00-00 | No | No | Current |
| 69306-050-09 | 69306005009 | 90 TABLET, FILM COATED in 1 BOTTLE (69306-050-09) | 2020-02-12 | 0000-00-00 | No | No | Current |