Ephedrine sulfate
- Product NDC
- 84549-611
- 11-digit product format
- 845490611
- Labeler code
- 84549
- Product ID
- 84549-611_3a38b027-e8ea-5d08-e063-6294a90a3b49
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ephedrine sulfate
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- ProPharma Distribution
- Application
- ANDA216129
- Marketing category
- ANDA
- Marketing start
- 2022-04-15
- Substance
- EPHEDRINE SULFATE
- Active strength
- 50 mg/mL
- Pharmacologic classes
- Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Increased Norepinephrine Activity [PE], Norepinephrine Releasing Agent [EPC], alpha-Adrenergic Agonist [EPC], beta-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
- Ephedrine sulfate
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| EPHEDRINE SULFATE | 50 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | U6X61U5ZEG |
| Rxcui | 1116294 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 84549-611-25 | Ephedrine sulfate | 1 mL in 1 VIAL, SINGLE-DOSE | 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 |
|---|
| 84549-611-25 | 84549061125 | 1 mL in 1 VIAL, SINGLE-DOSE (84549-611-25) | 1 ml | 2025-08-27 | No | No | Current |