rifampin
- Product NDC
- 70518-2404
- 11-digit product format
- 705182404
- Labeler code
- 70518
- Product ID
- 70518-2404_ecf6bc0b-744a-32ba-e053-2a95a90a156c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- rifampin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA090034
- Marketing category
- ANDA
- Marketing start
- 2019-11-05
- Marketing end
- 0000-00-00
- Substance
- RIFAMPIN
- Active strength
- 300 mg/1
- Pharmacologic classes
- Rifamycin Antibacterial [EPC], Rifamycins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2404-0 | 70518240400 | 30 CAPSULE in 1 BLISTER PACK (70518-2404-0) | 30 capsule | 2019-11-05 | 0000-00-00 | No | No | Current |
| 70518-2404-1 | 70518240401 | 30 CAPSULE in 1 BLISTER PACK (70518-2404-1) | 30 capsule | 2021-12-30 | 0000-00-00 | No | No | Current |