Vazculep
- Product NDC
- 51754-4010
- 11-digit product format
- 517544010
- Labeler code
- 51754
- Product ID
- 51754-4010_e457de4e-3de8-4cb9-9c1b-5e0ff5630f5b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenylephrine Hydrochloride
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Exela Phrama Sciences, LLC
- Application
- NDA204300
- Marketing category
- NDA
- Marketing start
- 2021-03-26
- Marketing end
- 0000-00-00
- Substance
- PHENYLEPHRINE HYDROCHLORIDE
- Active strength
- 10 mg/mL
- Pharmacologic classes
- alpha-1 Adrenergic Agonist [EPC],Adrenergic alpha1-Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51754-4010 | VAZCULEP (PHENYLEPHRINE HYDROCHLORIDE) INJECTION [EXELA PHRAMA SCIENCES, LLC] | 1 | Legacy NDC | 20210326_c73fc68d-6a3d-4d99-8869-cc64d7c6bf94.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51754-4010-4 | 51754401004 | 25 VIAL, SINGLE-DOSE in 1 CARTON (51754-4010-4) > 1 mL in 1 VIAL, SINGLE-DOSE | 2021-03-26 | 0000-00-00 | No | No | Current |