Phenylephrine hydrochloride
- Product NDC
- 84549-621
- 11-digit product format
- 845490621
- Labeler code
- 84549
- Product ID
- 84549-621_463d1c23-2403-026d-e063-6394a90a3bf4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- phenylephrine hydrochloride
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- ProPharma Distribution
- Application
- ANDA217069
- Marketing category
- ANDA
- Marketing start
- 2022-08-31
- Substance
- PHENYLEPHRINE HYDROCHLORIDE
- Active strength
- 10 mg/mL
- Pharmacologic classes
- Adrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Phenylephrine hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PHENYLEPHRINE HYDROCHLORIDE | 10 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 04JA59TNSJ |
| Rxcui | 1666372 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 84549-621-25 | Phenylephrine hydrochloride | 1 mL in 1 VIAL | INJECTION | 1 | | 3 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84549-621-25 | 84549062125 | 1 mL in 1 VIAL (84549-621-25) | 1 ml | 2025-08-27 | No | No | Historical |