Minocycline Hydrochloride
- Product NDC
- 70518-4565
- 11-digit product format
- 705184565
- Labeler code
- 70518
- Product ID
- 70518-4565_49ff6a70-4d73-b34a-e063-6394a90a338d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minocycline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA063065
- Marketing category
- ANDA
- Marketing start
- 2026-02-03
- 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
- 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 | 100 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 0020414E5U |
| Rxcui | 197984 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-4565-0 | Minocycline Hydrochloride | 28 in 1 BOTTLE, PLASTIC | CAPSULE | 28 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-4565-0 | 70518456500 | 28 CAPSULE in 1 BOTTLE, PLASTIC (70518-4565-0) | 28 capsule | 2026-02-03 | No | No | Current |