misoprostol
- Product NDC
- 72789-111
- 11-digit product format
- 727890111
- Labeler code
- 72789
- Product ID
- 72789-111_e65fd0bc-2fda-087c-e053-2a95a90a0108
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- MISOPROSTOL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- NDA019268
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2009-12-27
- Marketing end
- 0000-00-00
- Substance
- MISOPROSTOL
- Active strength
- 100 ug/1
- Pharmacologic classes
- Prostaglandin E1 Analog [EPC], Prostaglandins E, Synthetic [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 |
|---|
| 72789-111-08 | 72789011108 | 8 TABLET in 1 BOTTLE, PLASTIC (72789-111-08) | 8 tablet | 2020-09-04 | 0000-00-00 | No | No | Current |