Protriptyline Hydrochloride
- Product NDC
- 64980-159
- 11-digit product format
- 649800159
- Labeler code
- 64980
- Product ID
- 64980-159_995c0f12-2125-da56-e053-2995a90a8dfe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Protriptyline Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Rising Pharmaceuticals, Inc
- Application
- ANDA090462
- Marketing category
- ANDA
- Marketing start
- 2010-06-11
- Marketing end
- 0000-00-00
- Substance
- PROTRIPTYLINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 64980-159-01 | 64980015901 | 100 TABLET, FILM COATED in 1 BOTTLE (64980-159-01) | 2010-06-11 | 0000-00-00 | No | No | Current |