Misoprostol
- Product NDC
- 55154-4998
- 11-digit product format
- 551544998
- Labeler code
- 55154
- Product ID
- 55154-4998_b577b47a-56fc-458a-a004-ab2ce29064f0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Misoprostol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA091667
- Marketing category
- ANDA
- Marketing start
- 2013-07-16
- Marketing end
- 0000-00-00
- Substance
- MISOPROSTOL
- Active strength
- 200 ug/1
- Pharmacologic classes
- Prostaglandin E1 Analog [EPC],Prostaglandins E, Synthetic [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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55154-4998-0 | 55154499800 | 10 BLISTER PACK in 1 BAG (55154-4998-0) > 1 TABLET in 1 BLISTER PACK | 10 blister pack | 2013-07-16 | 0000-00-00 | No | No | Current |