DOXEPIN HYDROCHLORIDE
- Product NDC
- 70518-3017
- 11-digit product format
- 705183017
- Labeler code
- 70518
- Product ID
- 70518-3017_ec93f48f-3326-3fcd-e053-2a95a90a9f1e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DOXEPIN HYDROCHLORIDE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA213063
- Marketing category
- ANDA
- Marketing start
- 2021-02-05
- Marketing end
- 0000-00-00
- Substance
- DOXEPIN HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 70518-3017-0 | 70518301700 | 30 CAPSULE in 1 BLISTER PACK (70518-3017-0) | 30 capsule | 2021-02-05 | 0000-00-00 | No | No | Current |