Clarithromycin
- Product NDC
- 70518-1136
- 11-digit product format
- 705181136
- Labeler code
- 70518
- Product ID
- 70518-1136_b8b8bd2b-2c3f-4704-e053-2a95a90a39f1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clarithromycin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA203584
- Marketing category
- ANDA
- Marketing start
- 2018-04-25
- Marketing end
- 0000-00-00
- Substance
- CLARITHROMYCIN
- Active strength
- 500 mg/1
- Pharmacologic classes
- Macrolide Antimicrobial [EPC],Macrolides [CS],Cytochrome P450 3A4 Inhibitors [MoA],Cytochrome P450 3A Inhibitors [MoA],P-Glycoprotein Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1136-0 | 70518113600 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1136-0) | 2018-04-25 | 0000-00-00 | No | No | Current |