Ephedrine Sulfate
- Product NDC
- 70700-249
- 11-digit product format
- 707000249
- Labeler code
- 70700
- Product ID
- 70700-249_d3361dc6-a75e-ad9e-74fb-50965204eca3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ephedrine Sulfate
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Xiromed, LLC
- Application
- ANDA215825
- Marketing category
- ANDA
- Marketing start
- 2022-04-21
- 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 Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70700-249 | EPHEDRINE SULFATE INJECTION [XIROMED, LLC] | 1 | Current NDC | 20230413_8302176c-d443-97f1-1a49-12b9a204121a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 70700-249-23 | 70700024923 | 10 VIAL, SINGLE-DOSE in 1 CARTON (70700-249-23) / 1 mL in 1 VIAL, SINGLE-DOSE | 2023-04-11 | No | No | Current |
| 70700-249-25 | 70700024925 | 25 VIAL, SINGLE-DOSE in 1 CARTON (70700-249-25) / 1 mL in 1 VIAL, SINGLE-DOSE | 2023-04-11 | No | No | Current |