DOXEPIN HYDROCHLORIDE
- Product NDC
- 83209-638
- 11-digit product format
- 832090638
- Labeler code
- 83209
- Product ID
- 83209-638_214bbe66-8a57-61b3-e063-6294a90a10ba
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DOXEPIN HYDROCHLORIDE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Boswell Pharmacy Services LLC d/b/a BPS Wholesale
- Application
- ANDA215076
- Marketing category
- ANDA
- Marketing start
- 2024-09-04
- Substance
- DOXEPIN HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- DOXEPIN HYDROCHLORIDE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DOXEPIN HYDROCHLORIDE | 25 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3U9A0FE9N5 |
| Rxcui | 1000070 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 83209-638-30 | DOXEPIN HYDROCHLORIDE | 30 in 1 BLISTER PACK | CAPSULE | 30 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 83209-638-30 | 83209063830 | 30 CAPSULE in 1 BLISTER PACK (83209-638-30) | 30 capsule | 2024-09-04 | No | No | Historical |