Doxepin Hydrochloride
- Product NDC
- 70518-2371
- 11-digit product format
- 705182371
- Labeler code
- 70518
- Product ID
- 70518-2371_c8a92c7f-f965-7d1a-e053-2995a90ad8e4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxepin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA211603
- Marketing category
- ANDA
- Marketing start
- 2019-10-21
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2371-0 | 70518237100 | 30 CAPSULE in 1 BLISTER PACK (70518-2371-0) | 30 capsule | 2019-10-21 | 0000-00-00 | No | No | Current |