Desipramine hydrochloride 150 mg / 1 Tablet 50 Tablet
Reference details for licensed healthcare facility review and verification.
| NDC 11 | 50742-0117-50 |
|---|---|
| Product NDC | 50742-0117 |
| Generic Drug Name | desipramine hydrochloride |
| Brand Name | Desipramine Hydrochloride |
| Manufacturer | Ingenus Pharmaceuticals, LLC |
| Strength | 150 mg / 1 |
| Dosage Form | Tablet |
| Drug Type | Oral |
| Package Quantity | 50 Tablet |
| Package Description | 50 TABLET in 1 BOTTLE (50742-117-50) |
| Active Ingredients | Desipramine Hydrochloride |
| Marketing Category | ANDA |
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NDC snapshot
desipramine hydrochloride 150 mg / 1 Tablet is tracked under NDC 50742-0117-50 and rolls up into product family 50742-0117. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.
- Package configuration: 50 Tablet.
- Manufacturer: Ingenus Pharmaceuticals, LLC.
- Dosage form: Tablet.
- Family size: 1 indexed presentation.
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Official references
Use official labeling and directory references to confirm presentation details while your team reviews the PRN catalog entry and related sourcing paths.
Desipramine hydrochloride 150 mg / 1 Tablet 50 Tablet, NDC 50742-0117-50, is a Ingenus Pharmaceuticals, LLC 150 mg / 1 tablet presentation packaged as 50 Tablet.
NDC search formats
- Canonical NDC 11: 50742-0117-50
- Digits-only NDC 11: 50742011750
- Possible 10-digit display format: 50742-117-50 (5074211750)
Helpful product links
- Search by brand name: Desipramine Hydrochloride
- NDC 11: 50742-0117-50
- Product family NDC: 50742-0117
- VA classification code: CN601
- VA classification code description: TRICYCLIC ANTIDEPRESSANTS
- CMOP ID: D0017
- VUID: 4005628