Minocycline
- Product NDC
- 49884-512
- 11-digit product format
- 498840512
- Labeler code
- 49884
- Product ID
- 49884-512_6b95ec55-8686-495a-b24c-4e4409a5c2e8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minocycline
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Par Pharmaceutical, Inc.
- Application
- ANDA065131
- Marketing category
- ANDA
- Marketing start
- 2003-04-16
- Marketing end
- 0000-00-00
- Substance
- MINOCYCLINE HYDROCHLORIDE
- Active strength
- 75 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49884-512-01 | 49884051201 | 100 TABLET in 1 BOTTLE (49884-512-01) | 100 tablet | 2003-04-16 | 2023-01-31 | No | No | Current |