Minocycline Hydrochloride
- Product NDC
- 68071-4163
- 11-digit product format
- 680714163
- Labeler code
- 68071
- Product ID
- 68071-4163_bb632899-a753-7422-e053-2a95a90acc3a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minocycline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA063181
- Marketing category
- ANDA
- Marketing start
- 1991-12-30
- Marketing end
- 0000-00-00
- Substance
- MINOCYCLINE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Tetracycline-class Drug [EPC],Tetracyclines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 68071-4163-3 | 68071416303 | 30 CAPSULE in 1 BOTTLE (68071-4163-3) | 30 capsule | 2017-11-27 | 0000-00-00 | No | No | Current |
| 68071-4163-5 | 68071416305 | 15 CAPSULE in 1 BOTTLE (68071-4163-5) | 15 capsule | 2017-11-27 | 0000-00-00 | No | No | Current |
| 68071-4163-8 | 68071416308 | 28 CAPSULE in 1 BOTTLE (68071-4163-8) | 28 capsule | 2017-11-27 | 0000-00-00 | No | No | Current |