DOXEPIN HYDROCHLORIDE
- Product NDC
- 70518-2949
- 11-digit product format
- 705182949
- Labeler code
- 70518
- Product ID
- 70518-2949_dd29da8d-b409-8a95-e053-2995a90a922a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DOXEPIN HYDROCHLORIDE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA213063
- Marketing category
- ANDA
- Marketing start
- 2020-11-27
- Marketing end
- 0000-00-00
- Substance
- DOXEPIN HYDROCHLORIDE
- Active strength
- 75 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 |
|---|---|---|---|---|---|---|---|---|
| 70518-2949-0 | 70518294900 | 30 CAPSULE in 1 BLISTER PACK (70518-2949-0) | 30 capsule | 2020-11-27 | 0000-00-00 | No | No | Current |
| 70518-2949-1 | 70518294901 | 100 POUCH in 1 BOX (70518-2949-1) > 1 CAPSULE in 1 POUCH (70518-2949-2) | 100 pouch | 2021-07-13 | 0000-00-00 | No | No | Current |