PHENYLEPHRINE HYDROCHLORIDE
- Product NDC
- 50742-478
- 11-digit product format
- 507420478
- Labeler code
- 50742
- Product ID
- 50742-478_990a9dcd-2e1d-4ad4-a06d-ad48ae736f86
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PHENYLEPHRINE HYDROCHLORIDE
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Ingenus Pharmaceuticals, LLC
- Application
- ANDA209967
- Marketing category
- ANDA
- Marketing start
- 2020-01-16
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record