Sodium Bicarbonate
- Product NDC
- 72603-209
- 11-digit product format
- 726030209
- Labeler code
- 72603
- Product ID
- 72603-209_f2190c6c-50b8-4283-b715-1eabb7e4ff0f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SODIUM BICARBONATE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- NORTHSTAR RX LLC
- Application
- ANDA216364
- Marketing category
- ANDA
- Marketing start
- 2024-02-19
- Marketing end
- 2026-06-30
- Substance
- SODIUM BICARBONATE
- Active strength
- 84 mg/mL
- Pharmacologic classes
- Alkalinizing Activity [MoA]
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sodium Bicarbonate
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM BICARBONATE | 84 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8MDF5V39QO |
| Rxcui | 1868486 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72603-209-01 | Sodium Bicarbonate | 50 mL in 1 VIAL | INJECTION, SOLUTION | 50 | | 2 |
| 72603-209-25 | Sodium Bicarbonate | 25 in 1 CARTON | INJECTION, SOLUTION | 25 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72603-209 | SODIUM BICARBONATE INJECTION, SOLUTION [NORTHSTAR RX LLC] | 1 | Current NDC, 2 package rows | 20240219_068db1fe-0346-48f1-8d2f-8488d7331106.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72603-209-01 | 72603020901 | 50 mL in 1 VIAL | 50 ml | | | | | Historical |
| 72603-209-25 | 72603020925 | 25 VIAL in 1 CARTON (72603-209-25) / 50 mL in 1 VIAL (72603-209-01) | 25 vial | 2024-02-19 | 2026-06-30 | No | No | Historical |