Phenylephrine hydrochloride
- Product NDC
- 61990-0213
- 11-digit product format
- 619900213
- Labeler code
- 61990
- Product ID
- 61990-0213_a777109c-5929-4b97-9535-c9457fc9d797
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenylephrine hydrochloride
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Apollo Pharmaceuticals Inc.
- Application
- ANDA211081
- Marketing category
- ANDA
- Marketing start
- 2020-08-12
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61990-0213-1 | 61990021301 | 1 VIAL in 1 CARTON (61990-0213-1) > 10 mL in 1 VIAL (61990-0213-0) | 1 vial | 2020-08-12 | 0000-00-00 | No | No | Current |