Minocycline Hydrochloride
- Product NDC
- 70934-673
- 11-digit product format
- 709340673
- Labeler code
- 70934
- Product ID
- 70934-673_aa59137b-a1e1-b44b-e053-2995a90ac4ef
- 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
- 2020-04-22
- 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 |
|---|
| 70934-673-20 | 70934067320 | 20 CAPSULE in 1 BOTTLE, PLASTIC (70934-673-20) | 20 capsule | 2020-04-22 | 0000-00-00 | No | No | Current |