DOXEPIN HYDROCHLORIDE
- Product NDC
- 71335-2028
- 11-digit product format
- 713352028
- Labeler code
- 71335
- Product ID
- 71335-2028_a2974ea0-966c-4d3e-abd6-04323cb36f11
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DOXEPIN HYDROCHLORIDE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA213063
- Marketing category
- ANDA
- Marketing start
- 2020-07-01
- Marketing end
- 0000-00-00
- Substance
- DOXEPIN HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 71335-2028-1 | 71335202801 | 30 CAPSULE in 1 BOTTLE (71335-2028-1) | 30 capsule | 2022-02-10 | 0000-00-00 | No | No | Current |
| 71335-2028-2 | 71335202802 | 60 CAPSULE in 1 BOTTLE (71335-2028-2) | 60 capsule | 2022-02-10 | 0000-00-00 | No | No | Current |