DOXEPIN HYDROCHLORIDE
- Product NDC
- 16714-134
- 11-digit product format
- 167140134
- Labeler code
- 16714
- Product ID
- 16714-134_a422cc7f-3a62-46dc-91bd-7f8e392fb726
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DOXEPIN HYDROCHLORIDE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NORTHSTAR RX LLC
- Application
- ANDA213063
- Marketing category
- ANDA
- Marketing start
- 2020-07-01
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 16714-134 | DOXEPIN HYDROCHLORIDE CAPSULE [NORTHSTAR RX LLC] | 1 | Legacy NDC | 20201114_d7228639-25fa-4311-9241-11ad6af5c5e2.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 16714-134-01 | 16714013401 | 100 CAPSULE in 1 BOTTLE (16714-134-01) | 100 capsule | 2020-10-12 | 0000-00-00 | No | No | Current |