Doxepin
- Product NDC
- 72603-222
- 11-digit product format
- 726030222
- Labeler code
- 72603
- Product ID
- 72603-222_472f1364-17cc-0996-e063-6394a90aa786
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxepin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- North Star Rx LLC
- Application
- ANDA202337
- Marketing category
- ANDA
- Marketing start
- 2024-04-01
- Substance
- DOXEPIN HYDROCHLORIDE
- Active strength
- 3 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
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DOXEPIN HYDROCHLORIDE | 3 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3U9A0FE9N5 |
| Rxcui | 966787, 966793 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72603-222-01 | Doxepin | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72603-222 | DOXEPIN TABLET, FILM COATED [NORTH STAR RX LLC] | 5 | Current NDC, 1 package rows | 20250508_12edd5c6-c863-b83a-e063-6294a90a2f36.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72603-222-01 | 72603022201 | 30 TABLET, FILM COATED in 1 BOTTLE (72603-222-01) | 2024-04-01 | No | No | Current |