Minocycline Hydrochloride
- Product NDC
- 68151-2299
- 11-digit product format
- 681512299
- Labeler code
- 68151
- Product ID
- 68151-2299_e2eccf74-1ad0-48cb-a2f5-055830d1e81f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minocycline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- ANDA063065
- Marketing category
- ANDA
- Marketing start
- 1991-12-30
- Marketing end
- 0000-00-00
- Substance
- MINOCYCLINE HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Tetracycline-class Drug [EPC],Tetracyclines [CS]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68151-2299-5 | Minocycline Hydrochloride | 1 in 1 PACKAGE | CAPSULE | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-2299 | MINOCYCLINE HYDROCHLORIDE CAPSULE [CARILION MATERIALS MANAGEMENT] | 2 | Legacy NDC, 1 package rows | 20140708_00bf1ab3-dd22-439d-85fb-966dbb76c900.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68151-2299-5 | 68151229905 | 1 in 1 PACKAGE | Historical |