MINOCYCLINE HYDROCHLORIDE
- Product NDC
- 61919-337
- 11-digit product format
- 619190337
- Labeler code
- 61919
- Product ID
- 61919-337_94e4d98d-3f5d-a21b-e053-2995a90a38c2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- MINOCYCLINE HYDROCHLORIDE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA065062
- Marketing category
- ANDA
- Marketing start
- 2016-09-06
- 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
- 2020-12-31
- 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 |
|---|
| 61919-337-20 | MINOCYCLINE HYDROCHLORIDE | 20 in 1 BOTTLE | CAPSULE | 20 | | 3 |
| 61919-337-30 | MINOCYCLINE HYDROCHLORIDE | 30 in 1 BOTTLE | CAPSULE | 30 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-337 | MINOCYCLINE HYDROCHLORIDE CAPSULE [DIRECT RX] | 3 | Legacy NDC, 2 package rows | 20191101_3bdc5afb-63dc-4313-e054-00144ff8d46c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-337-20 | 61919033720 | 20 CAPSULE in 1 BOTTLE (61919-337-20) | 20 capsule | 2016-09-06 | 0000-00-00 | No | No | Current |
| 61919-337-30 | 61919033730 | 30 CAPSULE in 1 BOTTLE (61919-337-30) | 30 capsule | 2016-09-06 | 0000-00-00 | No | No | Current |