Minocycline Hydrochloride
- Product NDC
- 55695-004
- 11-digit product format
- 556950004
- Labeler code
- 55695
- Product ID
- 55695-004_2e0590da-df44-68ee-e054-00144ff8d46c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minocycline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Department of State Health Services, Pharmacy Branch
- 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
- 2019-12-31
- 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 |
|---|
| 55695-004-00 | Minocycline Hydrochloride | 100 in 1 BOTTLE, PLASTIC | CAPSULE | 100 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55695-004 | MINOCYCLINE HYDROCHLORIDE CAPSULE [DEPARTMENT OF STATE HEALTH SERVICES, PHARMACY BRANCH] | 3 | Legacy NDC, 1 package rows | 20160314_2b5f951e-4b70-2c1f-e054-00144ff8d46c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 55695-004-00 | 55695000400 | 100 in 1 BOTTLE, PLASTIC | Historical |