Minocycline Hydrochloride
- Product NDC
- 59651-339
- 11-digit product format
- 596510339
- Labeler code
- 59651
- Product ID
- 59651-339_2ef3b8ae-dd97-473f-bd81-c8c1b192c0ed
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minocycline Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Aurobindo Pharma Limited
- Application
- ANDA213662
- Marketing category
- ANDA
- Marketing start
- 2020-05-01
- Substance
- MINOCYCLINE HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Decreased Prothrombin Activity [PE], Tetracycline-class Drug [EPC], Tetracyclines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Minocycline Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MINOCYCLINE HYDROCHLORIDE | 100 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 0020414E5U |
| Rxcui | 207362, 207364, 403840 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 59651-339-50 | Minocycline Hydrochloride | 50 in 1 CONTAINER | TABLET, FILM COATED | 50 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59651-339 | MINOCYCLINE HYDROCHLORIDE TABLET, FILM COATED [AUROBINDO PHARMA LIMITED] | 3 | Current NDC, Legacy NDC, 1 package rows | 20250105_799a9871-3249-471e-b88d-5d8f7d4b96ad.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 59651-339-50 | 59651033950 | 50 TABLET, FILM COATED in 1 CONTAINER (59651-339-50) | 2020-05-01 | 0000-00-00 | No | No | Current |