Rifampin
- Product NDC
- 0143-9230
- 11-digit product format
- 001439230
- Labeler code
- 0143
- Product ID
- 0143-9230_1a816eb9-6de4-4751-831b-d183254f36af
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Rifampin
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Application
- ANDA205039
- Marketing category
- ANDA
- Marketing start
- 2016-03-03
- Substance
- RIFAMPIN
- Active strength
- 600 mg/1
- Pharmacologic classes
- Rifamycin Antibacterial [EPC], Rifamycins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Rifampin
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| RIFAMPIN | 600 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | VJT6J7R4TR |
| Rxcui | 312821 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0143-9230-01 | Rifampin | 1 in 1 VIAL | INJECTION, POWDER, LYOPHILIZED, | 1 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0143-9230 | RIFAMPIN INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [HIKMA PHARMACEUTICALS USA INC.] | 6 | Current NDC, Legacy NDC, 1 package rows | 20220210_cb59a48c-f66b-4ea0-809c-de0e4be2f8c2.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0143-9230-01 | 00143923001 | 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (0143-9230-01) | 2016-03-03 | 0000-00-00 | No | No | Current |