Misoprostol
- Product NDC
- 0904-6807
- 11-digit product format
- 009046807
- Labeler code
- 0904
- Product ID
- 0904-6807_07e58d46-ce43-4c8f-810c-3361a41e5a4e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Misoprostol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA091667
- Marketing category
- ANDA
- Marketing start
- 2012-07-25
- 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
- 2022-12-31
- 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 |
|---|
| 0904-6807-61 | 00904680761 | 100 BLISTER PACK in 1 CARTON (0904-6807-61) > 1 TABLET in 1 BLISTER PACK | 100 blister pack | 2012-07-25 | 0000-00-00 | No | No | Current |