Doxepin Hydrochloride
- Product NDC
- 71335-1450
- 11-digit product format
- 713351450
- Labeler code
- 71335
- Product ID
- 71335-1450_01ea9885-aec4-4f81-a11b-7aefd0fcc577
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxepin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA211603
- Marketing category
- ANDA
- Marketing start
- 2019-03-27
- Marketing end
- 0000-00-00
- Substance
- DOXEPIN HYDROCHLORIDE
- Active strength
- 10 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 Product Concepts#
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-1450-1 | 71335145001 | 30 CAPSULE in 1 BOTTLE (71335-1450-1) | 30 capsule | 2020-03-19 | 0000-00-00 | No | No | Current |
| 71335-1450-2 | 71335145002 | 60 CAPSULE in 1 BOTTLE (71335-1450-2) | 60 capsule | 2021-12-28 | 0000-00-00 | No | No | Current |
| 71335-1450-3 | 71335145003 | 18 CAPSULE in 1 BOTTLE (71335-1450-3) | 18 capsule | 2021-12-28 | 0000-00-00 | No | No | Current |
| 71335-1450-4 | 71335145004 | 90 CAPSULE in 1 BOTTLE (71335-1450-4) | 90 capsule | 2021-12-28 | 0000-00-00 | No | No | Current |
| 71335-1450-5 | 71335145005 | 180 CAPSULE in 1 BOTTLE (71335-1450-5) | 180 capsule | 2021-12-28 | 0000-00-00 | No | No | Current |