Doxepin Hydrochloride
- Product NDC
- 55700-783
- 11-digit product format
- 557000783
- Labeler code
- 55700
- Product ID
- 55700-783_368731a4-30b4-4b46-8268-61fdcd09a5f4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxepin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA211603
- Marketing category
- ANDA
- Marketing start
- 2019-08-09
- 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
- 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 |
|---|
| 55700-783-30 | 55700078330 | 100 CAPSULE in 1 BOTTLE (55700-783-30) | 100 capsule | 2019-08-09 | 0000-00-00 | No | No | Current |