Misoprostol
- Product NDC
- 68084-041
- 11-digit product format
- 680840041
- Labeler code
- 68084
- Product ID
- 68084-041_eb036f6e-7eb3-d8e7-e053-2a95a90a922b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Misoprostol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA091667
- Marketing category
- ANDA
- Marketing start
- 2013-07-08
- 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 |
|---|
| 68084-041-01 | 68084004101 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-041-01) > 1 TABLET in 1 BLISTER PACK (68084-041-11) | 100 blister pack | 2013-07-08 | 2021-11-30 | No | No | Current |