Isoniazid
- Product NDC
- 55695-033
- 11-digit product format
- 556950033
- Labeler code
- 55695
- Product ID
- 55695-033_2dcb1a5f-a1db-3686-e054-00144ff88e88
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Isoniazid
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Department of State Health Services, Pharmacy Branch
- Application
- ANDA080937
- Marketing category
- ANDA
- Marketing start
- 1972-09-01
- Marketing end
- 0000-00-00
- Substance
- ISONIAZID
- Active strength
- 300 mg/1
- Pharmacologic classes
- Antimycobacterial [EPC]
- 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 |
|---|
| 55695-033-00 | Isoniazid | 30 in 1 BOTTLE, UNIT-DOSE | TABLET | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55695-033 | ISONIAZID TABLET [DEPARTMENT OF STATE HEALTH SERVICES, PHARMACY BRANCH] | 2 | Legacy NDC, 1 package rows | 20160311_2b87aa05-8028-1b46-e054-00144ff8d46c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 55695-033-00 | 55695003300 | 30 in 1 BOTTLE, UNIT-DOSE | Historical |