Minocycline hydrochloride
- Product NDC
- 0440-7805
- 11-digit product format
- 004407805
- Labeler code
- 0440
- Product ID
- 0440-7805_bfa210b4-ad7a-48c0-9724-ee990117fef4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minocycline hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Liberty Pharmaceuticals, Inc.
- Application
- ANDA065062
- Marketing category
- ANDA
- Marketing start
- 2000-12-22
- Marketing end
- 0000-00-00
- Substance
- MINOCYCLINE HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Tetracycline-class Drug [EPC],Tetracyclines [CS]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 0440-7805-60 | Minocycline hydrochloride | 60 in 1 BOTTLE, PLASTIC | CAPSULE | 60 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0440-7805 | MINOCYCLINE HYDROCHLORIDE CAPSULE [LIBERTY PHARMACEUTICALS, INC.] | 1 | Legacy NDC, 1 package rows | 20131204_0b0cce68-5643-4239-82c7-105f5077a0e0.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 0440-7805-60 | 00440780560 | 60 in 1 BOTTLE, PLASTIC | Historical |