Phenoxybenzamine Hydrochloride
- Product NDC
- 66993-066
- 11-digit product format
- 669930066
- Labeler code
- 66993
- Product ID
- 66993-066_171ac5e5-5222-46ed-b048-b750fa366b67
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenoxybenzamine Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Prasco Laboratories
- Application
- NDA008708
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2015-08-11
- Marketing end
- 0000-00-00
- Substance
- PHENOXYBENZAMINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 66993-066 | PHENOXYBENZAMINE HYDROCHLORIDE CAPSULE [PRASCO LABORATORIES] | 14 | Legacy NDC | 20230707_29ddb739-0f8e-4c41-ab4b-a6331ae2d508.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 66993-066-02 | 66993006602 | 100 CAPSULE in 1 BOTTLE (66993-066-02) | 100 capsule | 2015-08-11 | 0000-00-00 | No | No | Current |