RANITIDINE
- Product NDC
- 53943-017
- 11-digit product format
- 539430017
- Labeler code
- 53943
- Product ID
- 53943-017_4799e029-69a9-4775-a653-22721865ae8e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- DISCOUNT DRUG MART
- Application
- ANDA207579
- Marketing category
- ANDA
- Marketing start
- 2017-11-13
- Marketing end
- 0000-00-00
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 75 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record