Misoprostol
- Product NDC
- 70710-1006
- 11-digit product format
- 707101006
- Labeler code
- 70710
- Product ID
- 70710-1006_8ccd806a-64c5-451e-89c9-f3920585a42f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Misoprostol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- Application
- ANDA210201
- Marketing category
- ANDA
- Marketing start
- 2020-01-14
- 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
- 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 |
|---|
| 70710-1006-1 | 70710100601 | 100 TABLET in 1 BOTTLE (70710-1006-1) | 100 tablet | 2020-01-14 | 0000-00-00 | No | No | Current |
| 70710-1006-4 | 70710100604 | 10 BLISTER PACK in 1 CARTON (70710-1006-4) > 10 TABLET in 1 BLISTER PACK (70710-1006-2) | 10 blister pack | 2020-01-14 | 0000-00-00 | No | No | Current |
| 70710-1006-6 | 70710100606 | 60 TABLET in 1 BOTTLE (70710-1006-6) | 60 tablet | 2020-01-14 | 0000-00-00 | No | No | Current |
| 70710-1006-8 | 70710100608 | 120 TABLET in 1 BOTTLE (70710-1006-8) | 120 tablet | 2020-01-14 | 0000-00-00 | No | No | Current |