# Tetracycline Hydrochloride

NDC: 51991-907
Generic name: Tetracycline Hydrochloride
Labeler / Manufacturer: Breckenridge Pharmaceutical, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20190118

FDA application: ANDA210662

## Active ingredients

- TETRACYCLINE HYDROCHLORIDE: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51991-907"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51991-907
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=00acf413-c5d2-4a54-9d0d-56266cbc9edc