Minocycline Hydrochloride
- Product NDC
- 72162-1840
- 11-digit product format
- 721621840
- Labeler code
- 72162
- Product ID
- 72162-1840_4909212c-308f-4322-b244-be6e7e506db8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minocycline Hydrochloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA204453
- Marketing category
- ANDA
- Marketing start
- 2016-09-30
- Substance
- MINOCYCLINE HYDROCHLORIDE
- Active strength
- 105 mg/1
- Pharmacologic classes
- Decreased Prothrombin Activity [PE], Tetracycline-class Drug [EPC], Tetracyclines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Minocycline Hydrochloride
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MINOCYCLINE HYDROCHLORIDE | 105 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 0020414E5U |
| Rxcui | 1013659 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-1840-3 | Minocycline Hydrochloride | 30 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 30 | | 104 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-1840 | MINOCYCLINE HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [BRYANT RANCH PREPACK] | 102 | Current NDC, 1 package rows | 20240918_99825095-d897-4077-86df-483d505615b2.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1840-3 | 72162184003 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1840-3) | 2016-09-30 | No | No | Historical |