Minocycline Hydrochloride
- Product NDC
- 63629-6422
- 11-digit product format
- 636296422
- Labeler code
- 63629
- Product ID
- 63629-6422_1149b9a0-c1dc-41fa-9bf9-06253627bd04
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minocycline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA063181
- Marketing category
- ANDA
- Marketing start
- 1992-02-01
- 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
- 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 |
|---|
| 63629-6422-1 | 63629642201 | 90 CAPSULE in 1 BOTTLE (63629-6422-1) | 90 capsule | 2015-09-17 | 0000-00-00 | No | No | Current |