Nitrofurantion
- Product NDC
- 70934-413
- 11-digit product format
- 709340413
- Labeler code
- 70934
- Product ID
- 70934-413_aefc0763-f18c-0675-e053-2a95a90af0ea
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nitrofurantion
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA201722
- Marketing category
- ANDA
- Marketing start
- 2019-07-19
- Marketing end
- 0000-00-00
- Substance
- NITROFURANTOIN
- Active strength
- 100 mg/1
- Pharmacologic classes
- Nitrofurans [CS],Nitrofuran Antibacterial [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-413-14 | 70934041314 | 14 CAPSULE in 1 BOTTLE, PLASTIC (70934-413-14) | 14 capsule | 2019-07-19 | 0000-00-00 | No | No | Current |