Minocycline hydrochloride
- Product NDC
- 70518-2943
- 11-digit product format
- 705182943
- Labeler code
- 70518
- Product ID
- 70518-2943_d79a5d6c-7543-807a-e053-2995a90a79fa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minocycline hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA063009
- Marketing category
- ANDA
- Marketing start
- 2020-11-17
- 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 |
|---|
| 70518-2943-0 | 70518294300 | 30 CAPSULE in 1 BOTTLE, PLASTIC (70518-2943-0) | 30 capsule | 2020-11-17 | 0000-00-00 | No | No | Current |