DOXEPIN HCL
- Product NDC
- 61919-863
- 11-digit product format
- 619190863
- Labeler code
- 61919
- Product ID
- 61919-863_8a81bc13-b35e-7b8d-e053-2995a90a1b09
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DOXEPIN HCL
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA207482
- Marketing category
- ANDA
- Marketing start
- 2019-06-05
- Marketing end
- 0000-00-00
- Substance
- DOXEPIN HYDROCHLORIDE
- Active strength
- 25 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-863-30 | 61919086330 | 30 CAPSULE in 1 BOTTLE (61919-863-30) | 30 capsule | 2019-06-05 | 0000-00-00 | No | No | Current |