DOXEPIN HYDROCHLORIDE
- Product NDC
- 68071-2356
- 11-digit product format
- 680712356
- Labeler code
- 68071
- Product ID
- 68071-2356_bd09f2b1-d809-9e27-e053-2a95a90a40ab
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DOXEPIN HYDROCHLORIDE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA213063
- Marketing category
- ANDA
- Marketing start
- 2020-07-01
- 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#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-2356 | DOXEPIN HYDROCHLORIDE CAPSULE [NUCARE PHARMACEUTICALS,INC.] | 2 | Legacy NDC | 20250112_bd0a04e2-cd1d-bd3f-e053-2995a90a7c81.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2356-1 | 68071235601 | 100 CAPSULE in 1 BOTTLE (68071-2356-1) | 100 capsule | 2021-03-08 | 0000-00-00 | No | No | Current |