Minocycline Hydrochloride
- Product NDC
- 70934-624
- 11-digit product format
- 709340624
- Labeler code
- 70934
- Product ID
- 70934-624_ab6cd2ea-5083-35e5-e053-2a95a90ac5cb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minocycline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. dba Northwind Pharmaceuticals
- Application
- ANDA065470
- Marketing category
- ANDA
- Marketing start
- 2020-03-16
- Marketing end
- 0000-00-00
- Substance
- MINOCYCLINE HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Tetracycline-class Drug [EPC],Tetracyclines [CS]
- 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 |
|---|
| 70934-624-30 | 70934062430 | 30 CAPSULE in 1 BOTTLE, PLASTIC (70934-624-30) | 30 capsule | 2020-03-16 | 0000-00-00 | No | No | Current |