Doxepin Hydrochloride
- Product NDC
- 68071-5260
- 11-digit product format
- 680715260
- Labeler code
- 68071
- Product ID
- 68071-5260_d772369c-f848-5d04-e053-2a95a90ab458
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxepin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA211603
- Marketing category
- ANDA
- Marketing start
- 2019-03-27
- Marketing end
- 0000-00-00
- Substance
- DOXEPIN 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
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 |
|---|
| 68071-5260-1 | 68071526001 | 100 CAPSULE in 1 BOTTLE (68071-5260-1) | 100 capsule | 2020-05-21 | 0000-00-00 | No | No | Current |