minocycline hydrochloride
- Product NDC
- 68071-5262
- 11-digit product format
- 680715262
- Labeler code
- 68071
- Product ID
- 68071-5262_d7727f40-9cdf-efef-e053-2995a90aa93f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- minocycline hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA063067
- Marketing category
- ANDA
- Marketing start
- 2017-10-31
- 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
- 2023-12-31
- 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 |
|---|
| 68071-5262-3 | 68071526203 | 30 CAPSULE in 1 BOTTLE (68071-5262-3) | 30 capsule | 2020-05-28 | 0000-00-00 | No | No | Current |