Doxepin hydrochloride
- Product NDC
- 70518-3496
- 11-digit product format
- 705183496
- Labeler code
- 70518
- Product ID
- 70518-3496_e6fdf437-1ffa-f4bf-e053-2995a90ab440
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxepin hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA212624
- Marketing category
- ANDA
- Marketing start
- 2022-08-24
- Marketing end
- 0000-00-00
- Substance
- DOXEPIN HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-3496 | DOXEPIN HYDROCHLORIDE (DOXEPIN HYDROCHLORIDE) CAPSULE [REMEDYREPACK INC.] | 2 | Legacy NDC | 20240113_4b59f6a5-1a14-45e1-aeba-cdf8a507305c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3496-0 | 70518349600 | 30 CAPSULE in 1 BLISTER PACK (70518-3496-0) | 30 capsule | 2022-08-24 | 0000-00-00 | No | No | Current |