misoprostol
- Product NDC
- 72789-128
- 11-digit product format
- 727890128
- Labeler code
- 72789
- Product ID
- 72789-128_e7176813-d1b6-5cf7-e053-2a95a90a98df
- 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
- 200 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 |
|---|
| 72789-128-04 | 72789012804 | 4 TABLET in 1 BOTTLE, PLASTIC (72789-128-04) | 4 tablet | 2020-10-07 | 0000-00-00 | No | No | Current |
| 72789-128-13 | 72789012813 | 13 TABLET in 1 BOTTLE, PLASTIC (72789-128-13) | 13 tablet | 2020-12-15 | 0000-00-00 | No | No | Current |