Phenylephrine hydrochloride
- Product NDC
- 42023-213
- 11-digit product format
- 420230213
- Labeler code
- 42023
- Product ID
- 42023-213_878d3299-4bf9-4c84-b6e6-d4fdbbe9093c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenylephrine hydrochloride
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Par Pharmaceutical, Inc.
- Application
- ANDA210025
- Marketing category
- ANDA
- Marketing start
- 2019-07-17
- Marketing end
- 2022-01-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42023-213-25 | 42023021325 | 25 VIAL, SINGLE-DOSE in 1 CARTON (42023-213-25) > 1 mL in 1 VIAL, SINGLE-DOSE | 2019-07-17 | 2022-01-31 | No | No | Current |