ranitidine 75
- Product NDC
- 0904-6715
- 11-digit product format
- 009046715
- Labeler code
- 0904
- Product ID
- 0904-6715_0b8b6ed2-7d1d-4d6d-86f9-0f86fb06b738
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA076195
- Marketing category
- ANDA
- Marketing start
- 2018-09-26
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0904-6715-46 | 00904671546 | 1 BOTTLE in 1 CARTON (0904-6715-46) > 30 TABLET, COATED in 1 BOTTLE | 1 bottle | 2018-09-26 | 0000-00-00 | No | No | Current |
| 0904-6715-52 | 00904671552 | 1 BOTTLE in 1 CARTON (0904-6715-52) > 60 TABLET, COATED in 1 BOTTLE | 1 bottle | 2018-09-26 | 0000-00-00 | No | No | Current |