AMITRIPTYLINE HYDROCHLORIDE
- Product NDC
- 60760-212
- 11-digit product format
- 607600212
- Labeler code
- 60760
- Product ID
- 60760-212_f06e6863-e0a1-584c-e053-2995a90a4851
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AMITRIPTYLINE HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA202446
- Marketing category
- ANDA
- Marketing start
- 2016-02-26
- Marketing end
- 0000-00-00
- Substance
- AMITRIPTYLINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60760-212 | AMITRIPTYLINE HYDROCHLORIDE TABLET, FILM COATED [ST. MARY'S MEDICAL PARK PHARMACY] | 6 | Legacy NDC | 20231209_60a4fa41-bf0b-7ea4-e053-2991aa0a0cd0.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-212-15 | 60760021215 | 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-212-15) | 2016-02-26 | 0000-00-00 | No | No | Current |
| 60760-212-90 | 60760021290 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-212-90) | 2019-10-15 | 0000-00-00 | No | No | Current |