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NDC 43063-0707-13 Misoprostol 200 ug/1 Details
Misoprostol 200 ug/1
Misoprostol is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by PD-Rx Pharmaceuticals, Inc.. The primary component is MISOPROSTOL.
MedlinePlus Drug Summary
Misoprostol is used to prevent ulcers in people who take certain arthritis or pain medicines, including aspirin, that can cause ulcers. It protects the stomach lining and decreases stomach acid secretion.
Related Packages: 43063-0707-13Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Misoprostol
Product Information
| NDC | 43063-0707 |
|---|---|
| Product ID | 43063-707_06486557-5c74-6d58-e063-6394a90adbac |
| Associated GPIs | 49250030000320 |
| GCN Sequence Number | 002767 |
| GCN Sequence Number Description | misoprostol TABLET 200 MCG ORAL |
| HIC3 | D4E |
| HIC3 Description | ANTI-ULCER PREPARATIONS |
| GCN | 08250 |
| HICL Sequence Number | 001187 |
| HICL Sequence Number Description | MISOPROSTOL |
| Brand/Generic | Generic |
| Proprietary Name | Misoprostol |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Misoprostol |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 200 |
| Active Ingredient Units | ug/1 |
| Substance Name | MISOPROSTOL |
| Labeler Name | PD-Rx Pharmaceuticals, Inc. |
| Pharmaceutical Class | Prostaglandin E1 Analog [EPC], Prostaglandins E, Synthetic [CS] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA091667 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 43063-0707-13 (43063070713)
| NDC Package Code | 43063-707-13 |
|---|---|
| Billing NDC | 43063070713 |
| Package | 13 TABLET in 1 BOTTLE, PLASTIC (43063-707-13) |
| Marketing Start Date | 2016-09-20 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |