Erythrocin Stearate
- Product NDC
- 24338-106
- 11-digit product format
- 243380106
- Labeler code
- 24338
- Product ID
- 24338-106_4a87d462-4bab-43ac-8003-4749f4219980
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ERYTHROMYCIN STEARATE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Arbor Pharmaceuticals, Inc.
- Application
- ANDA060359
- Marketing category
- ANDA
- Marketing start
- 2011-08-01
- Marketing end
- 0000-00-00
- Substance
- ERYTHROMYCIN STEARATE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Decreased Sebaceous Gland Activity [PE],Macrolide [EPC],Macrolide Antimicrobial [EPC],Macrolides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 24338-106-03 | 24338010603 | 30 TABLET, FILM COATED in 1 BOTTLE (24338-106-03) | 2019-08-31 | 0000-00-00 | No | No | Current |
| 24338-106-20 | 24338010620 | 100 TABLET, FILM COATED in 1 BOTTLE (24338-106-20) | 2011-08-01 | 0000-00-00 | No | No | Current |