Doxepin Hydrochloride
- Product NDC
- 68151-5656
- 11-digit product format
- 681515656
- Labeler code
- 68151
- Product ID
- 68151-5656_8abdb3d6-8491-48b1-99c7-d36b9e5664e1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxepin Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- ANDA074721
- Marketing category
- ANDA
- Marketing start
- 1998-12-29
- Marketing end
- 0000-00-00
- Substance
- DOXEPIN HYDROCHLORIDE
- Active strength
- 10 mg/mL
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68151-5656-7 | Doxepin Hydrochloride | 1 mL in 1 BOTTLE | SOLUTION | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-5656 | DOXEPIN HYDROCHLORIDE SOLUTION [CARILION MATERIALS MANAGEMENT] | 3 | Legacy NDC, 1 package rows | 20160213_83a42950-7b6f-4c86-b604-68e7f4c07859.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 68151-5656-7 | 68151565607 | 1 mL in 1 BOTTLE | 1 ml | Historical |