Misoprostol
- Product NDC
- 72789-121
- 11-digit product format
- 727890121
- Labeler code
- 72789
- Product ID
- 72789-121_d57d6ebb-f7fb-7ca0-e053-2995a90a7e6d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Misoprostol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA091667
- Marketing category
- ANDA
- Marketing start
- 2012-07-25
- 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
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72789-121 | MISOPROSTOL TABLET [PD-RX PHARMACEUTICALS, INC.] | 10 | Legacy NDC | 20241010_269a12db-b5a4-4beb-8c13-07f2ef6a58ec.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72789-121-08 | 72789012108 | 8 TABLET in 1 BOTTLE, PLASTIC (72789-121-08) | 8 tablet | 2020-09-24 | 0000-00-00 | No | No | Current |