phenylephrine hydrochloride
- Product NDC
- 36000-358
- 11-digit product format
- 360000358
- Labeler code
- 36000
- Product ID
- 36000-358_74192a42-0ff7-443b-9d8a-3096ef5c8e43
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- phenylephrine hydrochloride
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Baxter Healthcare Corporation
- Application
- ANDA217032
- Marketing category
- ANDA
- Marketing start
- 2026-04-06
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- phenylephrine hydrochloride
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PHENYLEPHRINE HYDROCHLORIDE | 10 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 04JA59TNSJ |
| Rxcui | 1232651, 1666372 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 36000-358-25 | phenylephrine hydrochloride | 1 mL in 1 VIAL, SINGLE-DOSE | INJECTION | 1 | | 1 |
| 36000-358-25 | phenylephrine hydrochloride | 25 in 1 CARTON | INJECTION | 25 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 36000-358-25 | 36000035825 | 25 VIAL, SINGLE-DOSE in 1 CARTON (36000-358-25) / 1 mL in 1 VIAL, SINGLE-DOSE | 2026-04-06 | No | No | Historical |